Download microsoft windows 10 jhu - seems magnificent
Welcome to Johns Hopkins Transcriptomics and Deep Sequencing Core Facility
Our aim is to provide cost-effective and time-efficient access to cutting-edge genomic technologies and expert assistance with experimental design and data analysis.
Our current service portfolio includes the following categories:
-Single Cell Sequencing: We offer single cell library preparation from both 10X Genomics and SplitBio. 10X Genomics is the foremost name in single cell sequencing. Library preparation methods are available for 3', 5', VDJ enrichment, and ATACseq protocols, each targeting up to 10, cells/sample. Multi-seq and cell-hashing multiplex samples to decrease library prep cost, while CITE-seq allows interrogation of both cell surface proteins and mRNA expression. Visium spatial gene expression ties histology and next-generation sequencng together, allowing users to map location of gene expression in tissue sections. Library prep and sequencing are available for Visium samples.
SplitBio targets up to , cells in up to 48 samples using combinatorial barcoding to uniquely tag individual cells. Cell populations are fixed prior to library prep to provide a more flexible alternative to fresh cell library preps.
Single cell libraries can be sequenced directly through the Core on the illumina NovaSeq, Illumina's most high throughput sequencer providing the lowest cost per base.
-NextGen Sequencing: we offer library constructions, for Illumina NovaSeq, HiSeq, NextSeq and MiSeq NextGen sequencing platform; and for various applications: mRNA-seq, ChIP-seq, ATACseq, single cell RNAseq, single cell ATACseq, single cell T-cell/B-cell receptor immune repertoire sequencing, Targeted Resequencing using Agilent Sure-Select Technology, and Microbiome 16S rRNA sequencing. We also offer complete service from library construction, through sequencing, and data analysis. NextSeq is our production power horse for its yield and short run time.-Third Gen Sequencing: We continue to offer library preparation, sequencing, and data analysis on PacBio Single Molecule Real-Time (SMRT) sequencing platform. As our RS II is down for now, sequencing can be run at other insitution's RS II or Sequel instruments. Such services includes short circular consensus sequencing for high accuracy for validating SNPs identified using other technologies, for determining mutation linkages, long reads sequencing for identifying potential new transcript isoforms, fusion genes, and chromosomal structure variations, and for helping sequence mapping with short reads especially for sequencing through regions with repetitive sequences. The techonology is extremely useful for de nove genome assembly, with the higher throughput of the new Sequel instrument, it has become more affordable to sequence any genome than before. We also offer Oxford Nanopore sequencing using MinIon. The flowcell yields upto 20Gb data and read length up to kbp. The library preparation is comparatively simpler than PacBio library prep and there is no size selection required. We have used Oxford Nanopore technology for de novo genome assembly for both bacteria and eukaryotic species.
We are now also offering Oxford Nanopore Sequencing on MinIon. The new single molecule sequencing platform for long read sequencing, another option for de novo genome assembly.
-Microarray: We are still offering Affymetrix microarray services. Our instrumentation for microarray analysis include an Affymetrix GeneChip Systems with autoloaders (capable of autoscanning 48 GeneChips each), four fluidic stations, one Affymetrix hybridization ovens. We also have an Agilent&#s most advanced 2-Micro Scanner and an Agilent hybridization oven for Agilent microarray services.
-Nanostring: We offer the Nanostring nCounter Analysis services for multiplexed gene expression, miRNA expression, and copy number variation analysis. The nCounter Analysis System utilizes a novel digital technology that use single molecule imaging to direcly counts the molecules without relying on enzymatic amplification. It requires a small amount of samples and offers high level of precision and sensitivity.
-DNA, Chromotin, and RNA shearing: The core offers sample shearing services using Covaris E instrument. The Covaris instrument uses ultrasonic wave with defined wavelength and Adaptive Focused Acoustics (AFA) technology to efficiently shear DNA, chromatin, or RNA to size distributions less than kb. Covaris is often used for library construction for short read sequencing.
-Data analysis: We offer statistical and bioinformatic data analysis on primary data and downstream functional analyses. We support data from our and other, outside, platforms; and can help with publication and database submission. We also provide commercial software at affordable rates for general use on our workstations or your own machine, either by subscription or by the hour. These software packages include Partek&#, Spotfire&#, and Ingenuity&# Pathway Analysis.
In addition, we also offer free pre-experimental consultation to ensure your study to be as successful as it can be, as economical as possible (we KNOW it's expensive!) and most importantly, as scientifically rewarding as possible.
The JHMI Transcriptomics and Deep Sequencing Core Facility is located on 3rd floor of Miller Research Building (MRB), formerly known as Broadway Research Building (BRB), in Room , and the lab in Room , just across the hallway. The core has been in operation since and has supported research projects from more than principle investigators and individual researchers. The core was initially funded by support from
- The School of MedicineOffice of the Dean
- Institute of Cell Engineering (ICE)
- Institute of Basic Biomedical Sciences (IBBS)
- McKusick-Nathans Institute of Genetic Medicine (IGM)
News
- Oct. 6th,
Announcing new LOWER prices for 10X library preparation! Price reduction is available on 3', 5' and ATACseq library preps (additional cost for CITE-seq, Multi-seq, cell-hashing, & VDJ enrichment libraries). Bulk discounts now available for as few as 2 samples, but you can earn significant cost savingg by processing 8 samples at a time. - Oct. 5th,
Direct client use of the Covaris sonicator is now available. No one-on-one training will be provided yet, but experienced users now have access to the instrument. - June 5th,
THE CORE HAS RE-OPENED! All services are available, with social distancing requirements. Appointmens are required for sample submission. Samples will be submitted with no contact, as clients may drop their samples in an ice bucket outside the lab. Covaris sonication is available, but the instrument is NOT available for individual use. Please consult directly with a Core member to arrange sonication. - Mar. 16th,
In accordance with University guideline, effective Wednesday, March 18th, the Transcriptomics and Deep Sequencing Core will be closed until further notice. No samples will be accepted as of this date. Any samples received prior to 3/18 will be stored and processed according to our queue once the univerisity returns to normal operation. Please help stop the spread of COVID virus by doing your part and stay healthy! - Mar. 13th,
Per University policy, the core is currently operating normally. We will let you know if situations change. To help stop or prevent COVID spreading, we encourage our users to use telecommunication as much as possible. We will be happy to consult and discuss data analysis over the phone and use Zoom or skype for sharing screens to facilitate discussion. Please stay safe and healthy during this difficult time. Thank you. - Mar. 11th,
Due to the COVID Pandemic, the Transcriptomics and Deep Sequencing Core Single Cell Symposium has been postponed until further notice. - Mar. 2nd,
We proudly present the Transcriptomics and Deep Sequencing Core Single Cell Symposium! The core Single Cell Sequencing Symposium will be held on April 20th, , at Tilghman Auditorium from am to pm. The symposium will present cutting edge research works by our users using single cell sequencing technology to address complex biological questions as well as various technologies for single cell sequencing and data validation. You can see the detailed announcement here and register for the symposium here. The preliminary symposium agenda can be viewed here. - Oct. 7,
Congratulations to Dr. Gregg Semenza on receiving this year's Nobel Prize in Physiology or Medicine for his groundbreaking discovery of a protein called hepoxia-inducible factor 1, or HIF HIF-1 helps cells cope with low oxygen levels, a key factor in health conditions such as coronary artery disease, chronic lung disease and cancer. See two of his publications in our publication list: PNAS (36), E and Cell Metab. 3(3), - Apr. 30,
Core Name Change To best reflect the services we mostly provide to the community, we are changing our name again from JHMI Deep Sequencing and Microarray Core to JHMI Transcriptomics and Deep Sequencing Core. The core began its life from early when we first started Affymetrix GeneChip microarray services and has been supported by the community continuously for more than 17 years. Many of our users has permanently associate the core with microarray and continue to fondly call the core "microarray core". We are proud of the fact and will continue to provide the same quality services the community has come to expect. To celebrate the continued success of the core and to thank the support of the community, we are celebrating with a 10% off offer to all projects submitted to our facility during the month of May (certain exclusions and restrictions apply, please talk to core staff for details). - Apr. 22,
Core Coin Notices The Johns Hopkins School of Medicine Core Corins Program has announced another round of funding. For calender year , core coin funding will be offered twice throughout the year (mid-year and end of calender year) and will be awarded directly to individual faculty to complete faculty-generated projects at any of the SOM cores using the iLab core management system. Our core is eligible for using core coins. Please apply for project that is already requested in iLab (ongoing project) or new project to be completed in our core at Core Coins Application. - Jan. 02,
New Prices for IPA and workstation usage. In the eight years that the Core has been providing discounted Ingenuity Pathway Analysis, IPA has contributed greatly to our colleagues' research, as seen in the Publications listed to the left. During this period increased usage has allowed us to hold the same price despite increases in what QIAGEN charges us. Our cost for represents an almost 60% increase from forcing us to increase what we charge colleagues to recover our costs. For this reason the cost of Ingenuity Pathway Analysis will increase to $ (from $) for a monthly private IPA account and $ (from $) per hour for Core workstation access. The good news is that our subscription now includes Comparison Analysis as well as isoform and GTEx project tissue-level expression datasets. We appreciate your continuing support and will continue to do all we can to hold our expenses down. - Jan. 02,
Happy New Year to all! Thanks to the continued support of our users, we had another successful year in with more than completed projects and 35 peer reviewed publications from our users (with 17 of those co-authored by core members). The core has added 10X Genomics Single cell RNAseq services and Oxford Nanopore MinIon sequencing to our service portfolio. These new services has produced a lot of interest in the community and expanded our user base. In we will continue to look out for new technologies and keep the core in the leading technologies to better serve the research community. In this spirit, we are happy to announce that the core is adopting Celsee Genesis single cell technology which offers the ability to gently capture and isolate individual cells up to , cells for proteogenomics, immune monitoring and single-cell transcriptomics. - Sept. 27,
Congratulations to Dr. Carlo Colantuoni for winning the core 10X Genomic Single cell RNAseq minigrant! Thanks to the support of 10X Genomics and Illumina, we instituted a minigrant to support one pilot study using 10X Genomics single cell RNAseq technique. The goal is to generate some preliminary data from the pilot study to enable grant application for future studies. Thanks to all who have participated in the minigrant competition! - June 1,
Oxford Nanopore Sequencing Service The core has started offering Oxford Nanopore Sequencing Services. Oxford Nanopore offers single molecule long reads that is suitable for genome assembly, cDNA sequencing, and 16s rRNA gene full length sequence. Oxford Nanopore technology is also capable of direct RNA sequencing, although currently the yield is much less than DNA or cDNA sequencing. In our initial test run with 1D sequencing, we generated 5Gb sequences. If you are interested in Oxford Nanopore technology, please come talk to us. - Feb. 27,
March Madness Promotion To celebrate March Madness, we are offering RNAseq for $ per sample! We will check the quality for each of the RNA samples (samples do not pass quality control may incur additional charges for QC), construct Illumina TruSeq stranded mRNA library (requires at least ng total RNA per sample), target 20 million single 75bp reads per sample, and analyze the data to detect differential gene expression (alignments and statistical differential detection where applicable). Additional down stream functional analysis (IPA and GO analysis) can be requested with additional cost! Submit your request through iLab and all samples need to be in core before March 31, - Nov. 2,
10X Genomic Single Cell RNAseq Services The JHMI Deep Sequencing and Microarray Core has obtained a 10X Genomic Single Cell RNAseq Instrument: 10X Genomics Chromium Single Cell controller. The system is up and running. Initial runs are successful with great results. 10X Genomics Single Cell RNAseq solution offers complete workflow from cell suspension through sequencing ready cDNA library in one day and has flexible throughput encapsulates ,+ cells in 10 minutes. Cell capture efficiency can be up to 65% and the library is compatible with Illumina HiSeq/NextSeq/MiSeq sequencers. We offer streamlined services including single cell encapsulation to data anlysis using 10X Genomics cellranger software and flexible to offer a la cart services as well. To use 10X Genomics Single Cell RNAseq service, please submit an iLab request and schedule with us to bring your cell suspensions to the core for immediate processing! - June 12,
Price Increase for sequencing services Due to vendor price increases, the core will be adjusting our service offerings related to Illumina NextSeq Mid Output runs and PacBio Sequencing SMRTcell sequencing. Some of the price increase has already been integrated into iLab listing and some are being integrated right now. All price changes are immediately and will affect new projects submitted into iLab from this point on! - Nov. 22,
Happy Holidays! The core has had another great year performing many services for our users. As always, we appreciate your choice to use our services and look forward to continued collaboration with you in next year. With the holiday season here, we want to keep your experiments running smoothly. Please note our holiday schedule and plan accordingly. We are closed Thursday Nov. 24th and Friday Nov. 25th for Thanksgiving Holiday and Friday Dec. 23rd through Monday Jan. 2nd for the Christmas and New Year Holiday. Thank you for your support and have a safe and happy holiday season! - Oct. 03,
Our second NextSeq instrument has been installed and up and running! With this we should have a very quick turn around for most of Illumina sequencing project. Hurrah!
Affymetrix Clariom class arrays are available through the core now! ClariomTM D and S arrays for human, mouse, and rat are newer versions of Affymetrix well established whole transcript array lines with updated probe designs for better performance and lower price. Clariom TM D arrays are new design for HTA and exon arrays while S arrays are newer design for Gene arrays. Moving forward, we would recommend the ClariomTM arrays over HTA/Exon or Gene arrays. - Aug. 30,
Second NextSeq instrument is being obtained. Due to popular demand on sequencing on NextSeq , we are experiencing some backlog despite our effort to running the instrument continuously. To improve the turn around time, we are actively pursuing to obtain a second NextSeq instrument. Hopefully, we will have the second instrument in the very near future and then it will improve our turn around time. Be patient! - July 1,
JHMI Deep Sequencing and Microarray Core iLab site is now the only way to request core services. To smooth core operation, we are requiring our users to submit a service request first before bringing samples to the core. We greatly appreciate your cooperation! - May. 2,
JHMI Deep Sequencing and Microarray Core iLab site is live! The iLab implementation for our facility has completed and the site is live. We will be transitioning service request from our old requisition forms to iLab. To ease the transition for our users, we will allow the concurrent use of either iLab service request or our current requisition form for two month. Coming July 1st, all service request will have all to be made through iLab. We would like to encourage you to sign-up for iLab and start using iLab for requesting your project. If you have difficulties, we would be happy to walk you through the service requesting process. - Apr. 21,
iLab implementation for JHMI Deep Sequencing and Microarray Core is almost completed! Exciting news! Our iLab implementation is almost finished. We hope by switching to iLab will streamline ordering and project progress tracking for our users. Currently the go live date is set to May 2nd. As the ilab goes live, there will be an initial time period that we will allow users to submit request using either iLab or our current requisition forms, but we strongly encourage everyone to register in iLab as eventually all request will go through iLab. In the coming days, more information will be provided here and on our web requisition forms. Stay tuned. - Feb. 5,
We have an Illumina NextSeq ! Today we have received our shipment of NextSeq instrument. This is exciting as the NextSeq can have similar throughput as HiSeq (comparing to per lane on HiSeq ) and the turn around time is just merely one day. This will improve our Illumina sequencing turn around time significantly. Cheers! - Jan. 8,
Happy New Year! The JHMI Deep Sequencing and Microarray Core would like to take this opportunity to thank everyone for your continued support and business. Last year, the core and our users have had another successful year. By our counting, there have been 28 publications by our users so far, with 10 of them coauthored by core members (see our publication list here). Congratulations to everyone and wish everyone a most successful year in ! The core will continue to improve our services and with the new year, more changes is coming. Check back soon for more details!. - Nov,
We are implementing iLab In the next two month, we will implement iLab lims in our core. Once the implementation completes, we will transition all our requistion process to iLab. Hope that will streamline the process of requesting services from the core. - Nov. 12,
Our PacBio RS II can run 6 hr movies now (previously four hour movie) and generates >1G data per run! - Apr. 6,
Due to Illumina price hike, we are adjusting our price related to illumina sequencing and the new price is effective immediately. - Sept. 26,
PacBio RS II sequencing price increase After reviewing the cost recovery rate for PacBio RS II sequencing services, we have found it necessary to increase the price for our PacBio RS II sequencing services to ensure the sustainability of the service. The new price will take effect immediately for any new project and future adjustment possible if further review indicates the necessity. - Jun 5,
PacBio SMRTest MICROBE GRANT PROGRAM For your information, PacBio is running a small research grant program that offers upto 4 smrtbell libraries and 8 smrtcell sequencing on microbe (covering all reagents and consumables). Here is a link for you to submit your entry by June 15, - Jun. 27,
Core Service Rate Increase For the last few years, we have maintained our rate constant. However due to increased cost for us, we have to institute a rate increase to keep us from loosing money. The new rate is now in our rate schedule and the new rates are effective immediately. The rate increase will not affect projects that is being processed in the core lab, in the core lab queue, or being analyzed in the analysis unit. Any new project will be charged using the new rate. - Sept. 10,
MiSeq Upgrade. Our MiSeq instrument has been upgraded so that it can now run 2X cycle runs and it also doubled the output for 2X and 1X50 cycle runs. - Aug. 30,
Perkin Elmer/Caliper GXII high throughput LabChip system. The JHMI Deep Sequencing and Microarray Core now has a Caliper GXII high throughput LabChip system with abilities to run quality control on hundreds of RNA, DNA, and protein samples. - July 2,
NanoString $10K reagent grant competition! NanoString has just announced that they are having a grant competition. Please see the flyer for details. We have the nCounter systems in our facility and will be able to provide services on all Nanostring assays including gene expression, miRNA, epigenomics, and copy number variation assay. - June 7,
Automated Sequencing Library Preparation! We have purchased a Nugen Mondrian SP system thanks to funding from Johns Hopkins Brain Science Institute. The Nugen Mondrian SP System provides an automation solution for sequencing library preparation and offers the ability to generate library from limited amount of DNA (down to 1 ng). This capability opens a whole field of studies that were previously not amenable. Happy Sequencing!. - May 10,
We have a MiSeq Now! Thanks to Dr. Nancy Craig and HHMI, now the core has an Illumina MiSeq - a fully integrated personal sequencer with a streamlined solution that offers rapid sample prep, push-button fast sequencing and automated data analysis. The MiSeq currently is capable of generating up to 2 Gb of sequence data per run and will soon be able to generate up to 7 Gb of data. It is an excellent option for targeted resequencing, small genome sequencing, RNA sequencing, ChIP sequencing and Methylated sequencing. With single lane and fast chemistry, MiSeq offers a quick turn around from library preparation to sequencing data. For our service rate, please see the rate schedule. - Mar. 15,
Affymetrix introduces Whole-transcriptome analysis Gene ST arrays for 16 model organisms including Arabidopsis, Bovine, Canine, Chicken, Cynomolgus, Equine, Feline, Marmoset, Medicago, Ovine, Porcine, Rhesus, Rice, Soybean, Zebra Finch, and Zebrafish. For details, please see Model and applied research organisms Gene ST Array for details. These arrays are now available in cartridge array format that we can process in our lab. - Sept. 28,
Introducing Affymetrix New Human PrimeView Gene Expression Array: Affymetrix has introduced a new low cost 3 prime gene expression array for research purpose. The new array is called Human PrimeView Gene Expression Array and it covers all confirmed transcribed genes and variants (total transcripts for gene expression and alternate 3' end of well annotated genes. Please see Affymetrix Web Site for details. - Aug. 30,
PacBioRS is in the Core: The PacBio RS instrument has arrived in the core. PacBio engineers are working on installing and testing the instrument to have it up and running. For more information on PacBio RS instrument, please visit Pacific Biosciences Company web site. Come back for more update on PacBio RS instrument! - May 6,
PacBioRS is coming to the core: With the support from School of Medicine Office of the Dean, the core has purchased a PacBio RS third generation single molecule sequencer. The instrument is capable of long read (currently reported read length average kb) which will benefit sequencing through repetitive sequences. Other potential application of the instrument include direct detection of DNA methylation and direct RNA sequencing. The expected delivery date of the instrument is late in the summer. Check back to get updated information on PacBio RS sequencer! - Jul. 20,
Our Core has a new name: To reflect the new service offering and directions the core is taking, we have changed our name to JHMI Deep Sequencing and Microarray Core! - Jul. 20,
New NanoString nCounter Analysis System: Thanks to a research grant from Johns Hopkins Brain Science Institute, JHMI Deep Sequencing and Microarray Core Facility has acquired a NanoString nCounter Analysis System. The NanoString nCounter Analysis System is the first and only technology platform to deliver highly multiplexed, direct detection and counting of individual molecules in a single reaction without amplification. The first applications for the nCounter Analysis System offer cost-effective ways to easily profile hundreds of gene transcripts, micoRNAs, or genomic copy number variants simultaneously with high sensitivity and precision. This effectively bridges the gap between discovery technologies such as microarrays, and single-plex technologies like real-time PCR. The system includes a fully automated sample Prep Station, a Digital Analyzer, the CodeSet (molecular barcodes) and all reagents needed to perform the analysis. Assay panels are currently available for gene expression analysis, miRNA analysis, and Copy Number Variation analysis. For informations on how to access NanoString nCounter Analysis Systems, please contact us. - Jul. 8,
NextGen Sequencing Price Online: We have updated our price to include library preparation and Illumina sequencing service fees. Our library preparation service offers low cost (same price as reagent cost from illumina) and high quality results (we have obtained 50 million reads from paired-end sequencing with approximately more than 80% alignable reads). Please contact us to discuss your NextGen sequencing needs. - Jul. 8,
We have a new server: Thanks to the generosity of Stanley Medical Research Institute, JHMI microarray core now possess a linux based server with dual Quad core processor, 48 GB RAM, and terabyte storage space for supporting data analysis on large data sets including nextgen sequencing data. - Jul. 8,
CLC Genomics Server and Workbench: Thanks to the generosity of CLC Bio, we have installed CLC Genomics Server and CLC Genomics Workbench on a trial basis for analyzing NextGen sequencing data. The Genomics Workbench runs on Macintosh, WIndows and Linux computers, and it imports data from SOLiD, Illumina, , and Helicos. Functions in the Workbench include, quality and adapter trimming, de novo assembly, reference assembly, RNA-seq, ChIP-Seq, SNP and DIP detection, and a suite of functionality for microRNA analysis. The Genomics Server allows you to analyze your data with the tools from the Genomics Workbench, but on a remote machine, one with much greater processing power, such as our new server. The Genomics Workbench accesses the Genomics server as a thick client, so you can process your data from your office, but much more efficiently than your desktop computer can. For testing out the CLC Genomics Server or Workbench, please contact Conover Talbot Jr. or Haiping Hao. - Jul. 8,
New price effective immediately: To ensure that we do not operate at a loss and to reflect our cost changes, we have implemented a price adjustment on Affymetrix arrays. Any new project submitted from July 7, and forward will be subjected to the new service fees. To minimize the impact of the price change, we have lowered our quantity discount requirement so that projects with 10 or more samples will enjoy a considerable discount as compared to 24 or more samples previously. - Jan. 1,
Happy New Year from the Core: New Services for the new year - NextGen sequencing, NextGen sequencing library construction, high-throughput sonication using Covaris&# E instrument. - May 12,
Hybridization unit new services: Affymetrix Genome-wide human SNP / arrays, human mapping K and K array sets, drug metabolism biomarker panel DMET Plus array, multiorganism miRNA arrays; Agilent 1 million feature G3 SurePrint Human aCGH arrays. - May 1,
The monthly charge for using Spotfire has been reduced to $ per month. - Feb. 5,
Partek Genomics Suite version is available on core workstations in BRB - Jan. 5,
New pricing/fee schdule for is available. - May 1,
New version of Spotfire is available. Interested users please contact Microarray Core or fill out a account request form. - March 1,
Partek Genomics Suite is available on the workstations in Room BRB; - Febuary 1,
Microarray core hybridization unit announces new lower prices for our most popular array services and new services added to our portfolio. - November 1,
Microarray Core computer room (BRB ) has the latest version of Stratagene software installed, ArrayAssist and PathwaArchitect . - Ocbober 29,
Welcome Haiping Hao!
Dr. Haiping Hao is the new manager for the Microarray Core Lab. - October 9,
Analysis Unit institutes a much needed rate hike on Oct 10, to help meet its costs. The new rate for consultation and analysis requests is $85/hr. - April 5,
PathArt has been upgraded to Release 1.Go to JHMI Microarray Core's PathArt Server. (within Hopkins networks only) - Jan. 16,
PathwayArchect and ArrayAssist Software Packages (from Stratagene) are accessible from Hopkins campuses. Details in the software page; - Jan. 9,
We are now running PathArt R4. Go to JHMI Microarray Core's PathArt Server. (within Hopkins networks only) - Aug. 20,
PathArt R2 is available within Hopkins campuses. - May 2,
GeneSpring license renewed and license server software upgraded; GeneSpring Users can upgrade to GeneSpring GX ; - June 15,
JHMI Microarray Core has started running its own Spotfire DecisionSite Server version . Interested users should refer to the How to download and install Spotfire document for details about its access. - Dec,
Affymetrix announces changes in array production of older generation of GeneChip&#, U95, U34, U74,etc.. See details; - Nov. 17,
A new way to access GeneSpring License Server, that will avoid the Mutiple session message that stops GeneSpring running on your desktop. Please read the GeneSpring installation docs for Microsoft Windows or Mac OS X for details. - May 15,
Hybridization Lab moves to Room BRB. JHMI Microarray Core Facility is in a single location now! - March 26,
Analysis Unit moves to Room , Broadway Reserch Building (BRB). - Feb. 25,
New requistion form online! - Feb. 16,
Microarray Core's FTP site launched! Users who have used hybridization unit can download their data. For details please click here or the "FTP server" link on the left menu. - Jan. 8, Analysis Unit has moved to Room , Broadway Research Building. Most of the services (including Microarray core facility web site and GeneSpring license server) are back to normal.
- Analysis Unit has moved!
Starting 12/16/03, Microarray Core's Analysis Unit is moving from its Jefferson rushbrookrathbone.co.ukng location to the its temporary quarter located at Broadway Research Building (BRB) room - 7/16/03, 9ampm - Microarray Core hosts the BioDiscovery "Statistical Analysis of Gene Expression for Microarray Data" seminar.
- 12/04/02 - Microarray Core hosts the Spotfire for Microarray Data Analysis presentation.
- 10/28/02 - 10/29/02 - Microarray core presents the BioConductor Workshop for Microarray Data Analysis.
- 9/3/02 - Analysis Unit starts to offer services on a trial basis for free! We provide both the access and technical help for some of the most popular packages like GeneSpring, Spotfire, and Biodiscovery suite (ImaGene and GeneSight) . You can find more details under the software menu on the left.
- 1/30/02 - Official opening Microarray Core
- 1/09/02 - Hybridization Unit initiates service
Last modified: Mon Oct 12
-
-