Subscribe to the RNA-Seq Blog
Featured Events
.png)
Media Partners
Polls
Loading ...
Auto req
18388BR
Job Posting Title
Scientist - Genome Analysis Unit
Career Category
Scientific
Employee Subgroup
Salaried…
Bioinformatician
1370806
CLARiENT, a GE Healthcare company
At Clarient, we combine innovative diagnostic technologies with world-class pathology…
Please feel free to contact me at bhamory@theranos.com
Theranos is actively building a world-class team. Ideal candidates are currently employed or…
The group “Systems Biology of the Cellular Microenvironment” at the Institute for Molecular Medicine and Cell Research (IMMZ), U, is…
Job Description
Xylo Technologies Inc. is an established Information Technology organization that serves Fortune and Mid-Tier corporations. Xylo has…
Job Number:
83192857
Company Name:
Infinity Pharmaceuticals, Inc.
Location:
Cambridge, MA US
Career Focus:
Management &…
Supervisors
Dr Qiongyi Zhao qiongyi.zhao@uq.edu.au
Dr Kostya Shakhbazov k.shakhbazov@uq.edu.au
A/Prof Naomi Wray…
Position Title: SCIENTIST (Computational Biologist) Grade 26
Position ID: 1281130206
Description
Johnson & Johnson Pharmaceutical…
Research Associate III Baylor Research Institute Dallas Bioinformatics\Computational Biology Weekday
Job Number:
81099147
Company…
Postdoctoral Researcher (Molecular Genetics) Primordial Dwarfism and Organism Growth
School of Molecular, Genetic and Population Health…
Job Number:
79287699
Company Name:
Pfizer Inc.
Location:
Cambridge, MA US
Career Focus:
Information Technology / Science &…
Computational Biologist - Novartis Pharmaceuticals (United States)
…in cell or molecular biology .Expertise in genomic data analysis -…
Intern Product Development
Job Location: Austin, TX
The successful candidate will support product development activities for gene expression…
Belgian Nuclear Research Center
Mol, Belgium
Development of a RNA-seq analysis pipeline for bacterial transcriptomics
Introduction/framework…
The Opportunity:
The Morgridge Institute for Research seeks a Computational Biologist to provide bioinformatics support to researchers studying…
Senior Scientist / Principal Scientist, Immunoregulation
Job Number:
971088
Company Name:
Pfizer Inc.
Location:
Cambridge, MA…
Senior Application Scientist
Location:
Redwood City, CA
Job Code:
120146
# of…
Postdoctoral Bioinformatician
Nuffield Department of Medicine (NDM), Ludwig Institute for Cancer Research, Old Road Campus Research Building,…
Job Number: 165654
Category: A -…
Statistical analysis of RNA-seq data from next-generation sequencing experiments of cancer.
Institution: Queen’s University… 
Featured RNA-Seq Job – Scientist – Genome Analysis Unit – Amgen
Featured Job – Bioinformatician – GE (United States)
Theranos is currently looking for scientists with solid RNA Sequencing experience
Post-Doc Position in Systems Biology and Modeling of High-Throughput Data – Freiburg, Germany
Featured RNA-Seq Job – Bioinformatics rna-seq proteomics Java developer
RNA-Seq Summer Internship – Computational Biology
PhD Position Available – Analyzing alternative splicing events in human transcriptome sequencing data
Featured RNA-Seq Job – Computational Biologist
Featured RNA-Seq Job – Research Associate III Baylor Research Institute Dallas Bioinformatics\Computational Biology
Featured Job – Postdoctoral Researcher (Molecular Genetics) Primordial Dwarfism and Organism Growth
Senior / Principal Scientist / Data Analyst – Exploratory
Featured RNA-Seq Jobs
Internship Available – Product Development – RNA-Seq
Master thesis – Bioinformatics – RNA-Seq analysis
Featured RNA-Seq Job – Computational Biologist
Featured Job – Senior Scientist – Pfizer
Featured Job Listing – Senior Application Scientist – Ingenuity Systems
Available Postdoctoral Position – RNA-Seq
Featured Job Opening – Bioinformatics Scripter within Production Bioinformatics
Available PhD Research Project – RNA-Seq
Incoming search terms:
- rna seq analysis jobs
- RNA seq analysis job
- job rna seq data analysis
- Phd position RNA seq analysis USA
- jobs rnaseq
- jobs rna
- pfizer postdoc rnaseq
- Trinity RNA-seq memory
- RNA-SeqJobs|RNA-SeqBlog
- rna-seq jobs
Social Networking Pages
-
SEQanswers – RNA Sequencing- The Transcript Length from Cufflinks May 25, 2013Hi Guys, I'm doing a fungus RNA-Seq.However, the merged transcriptome gave me very long transcripts (generally >2K). I used GeneMarES to do... […]hchang10
- DESeq; can I omit timepoints during dispersal estimation? May 24, 2013I have a bacterial timecourse with 2 biological replicates per timepoint. There is a fair bit of variance between my replicates. I have spent the... […]amcloon
- HT Seq Count stranded options May 24, 2013I am very new to bioinformatics, so I would be really grateful for some help! I have been using *HTSeq Count v0.5.3* and I am bit confused about... […]qwrissie
- Tophat 2.0.8b installation error May 24, 2013I install tophat-2.0.8b to rerun the mapping. but when i make it, the error appears like this. make[1]: Entering directory... […]canhu
- reason for low mapping rate?? May 23, 2013we did RNASeq using HiSeq 2000 100PE. When the data were back, I mapping them to the reference sequence, but got very low mapping rate (30-40%). I... […]miaom
- cross-species data - questions about normalization May 23, 2013Hi, I have some data form various samples (cell types) in different species. I want to compare and analyze gene expression variability across the... […]trelek2
- The Transcript Length from Cufflinks May 25, 2013
- Biostar – RNA-Seq
- Why am I getting so many unmapped reads in STAR, classified as "too short"?I am currently using STAR to map several Hi-SEQ mRNA runs. I'm having trouble getting a decent amount of reads to map, but I don't really understand why. I'm hoping you can shed some light :) In the final log, only about 50% (or less) of the reads map to the reference. I'm using a GTF in addition to the genome. The unmapped bin that most […]
- What are the best practices for SNP identification in RNA seq transcriptome dataI have 20 RICE RNA seq tranascriptome data hiseq 2000 platform paired end reads. I aligned fasta reads with BWA and remove PCR duplicates with PICARD. Later I call SNP with samtools using various parameters. I would like to clarify what parameters should I used while alinging to reference rice genome for looking SNP location 100 bp upstream and 250 bp downst […]
- How do TopHat options -g , --supress-hits, and Bowtie options interplay?Hi, I am currently using TopHat2 to map RNA-seq runs. I think there have been some changes pertaining the -g option. Does anyone know how it works now? I used to think that setting -g would look for n alignments for a given read, report them [if top-scoring] and discard those reads that had more than g [top scoring] alignments. Now, the description sounds mo […]
- What happened to -k in TopHat for multiple-mapping reads?Selecting -g n in tophat does not discard reads mapping more than n, but instead only reports n alignments for those out all all their TOP scoring alignments. I think there used to be an option -k that would allow one to discard reads that topped x alignments -- whatever happened to that? I only see -g in the tophat 2 manual, no reporting options like before […]
- Does tophat use the library-type information for mapping, or just for the XS flag?When I specify library-type to TopHat, i.e., first-strand, second-strand, unstranded, TopHat appends a value + or - to the XS:A flag, which is useful for subsequent analyses, such as annotation. However, does this information actually influence the "mappability" of reads, or is this unaffected? My thinking is that the information would be considere […]
- Purpose of Y-shaped adapters in Illumina Sequencing?Hi all, Y adapters different sequences to be annealed to the 5' and 3' ends of each molecule in a library. The arms of the Y are unique, and the middle part, connected to the DNA fragment, is complementary. What are the advantages of this? My take of this over having fully-complementary adapters (ADAPTER1 - - - - - ADAPTER1) is that: -Upon primer a […]
- Why am I getting so many unmapped reads in STAR, classified as "too short"?