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5
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Answer: A: A Question On Grouping Into Rna,Trna,Rrna,Sntna,Scrna,Snorna,Lincs.Etc
updated 4.6 years ago by 43k • written 12.5 years ago by 19k
3
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0
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8.4k
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Answer: A: Rna-Seq Data Analysis & Good Review/Research Article On Same
updated 4.6 years ago by 43k • written 12.2 years ago by 19k
42
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17
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38k
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15 follow
Forum: List Of Genome Sequencing Centers/Institutes
genomics institutes
updated 14 months ago by 43k • written 11.2 years ago by 19k
4
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0
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1.2k
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News: Workshop for genomic data visualization and interpretation
R RNA-Seq ggplot2 genomics
updated 10 months ago by 43k • written 5.3 years ago by 19k
0
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0
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5.8k
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Comment: C: Web Resources To Find Cancer Indication Where A Given Gene Is Amplified
updated 5.2 years ago by 43k • written 9.1 years ago by 19k
2
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1
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39k
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Answer: A: Combining Data Of Multiple Vcfs Into One.
updated 5.3 years ago by 43k • written 10.9 years ago by 19k
4
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1
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1.5k
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Job: Cancer Genomics and Bioinformatics positions at WashU (Griffith Lab)
Cancer Immunogenomics
updated 10 months ago by 43k • written 5.3 years ago by 19k
17
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11
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12k
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8 follow
What Is The Fastest Method To Determine The Number Of Positions In A Bam File With >N Coverage?
bam bedtools samtools coverage depth-of-coverage depth-of-coverage
updated 5.5 years ago by ★ 1.5k • written 10.9 years ago by 19k
0
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0
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123k
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Comment: C: Where Can I Download Human Reference Genome In Fasta Format? Hgref.Fa File
updated 5.6 years ago by 43k • written 9.8 years ago by 19k
2
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1
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31k
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Answer: A: What Methods Do You Use For In/Del/Snp Calling?
updated 5.6 years ago by 43k • written 12.2 years ago by 19k
0
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0
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69k
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Comment: C: Recommend Your Favorite Bioinformatics Books
updated 5.6 years ago by 43k • written 8.5 years ago by 19k
48
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4
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30k
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Answer: Answer: Drug to Target/Gene/Protein Interaction Databases
updated 2.6 years ago by 43k • written 12.2 years ago by 19k
1
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0
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1.9k
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Comment: C: Comprehensive & integrated drug/target database?
6.1 years ago by Malachi Griffith 19k
2
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1
reply
15k
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Comment: C: Exploring cancer mutation data portals
6.2 years ago by Malachi Griffith 19k
1
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1
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15k
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Comment: C: Exploring cancer mutation data portals
6.3 years ago by Malachi Griffith 19k
18
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8
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6.6k
views
6 follow
Publicly Available Tumor/Normal Illumina Data For Evaluation Of Somatic Variant Callers
variant somatic
updated 22 months ago by 43k • written 11.5 years ago by 19k
27
votes
12
replies
11k
views
Tool: Skewer: a fast and accurate adapter trimmer for next-generation sequencing paired-end reads.
QC Trimming Read Trimmer
updated 2.5 years ago by 43k • written 9.8 years ago by 19k
0
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0
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3.5k
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Comment: C: Liftover Of Na12878 Coordinates Into Hg19 Coordinates
6.6 years ago by Malachi Griffith 19k
0
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0
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5.8k
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Comment: C: Updating dbSNP rs ids from old SNP data
6.6 years ago by Malachi Griffith 19k
0
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0
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145k
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Comment: C: Converting Genome Coordinates From One Genome Version To Another (Ucsc Liftover,
6.6 years ago by Malachi Griffith 19k
0
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0
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22k
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Comment: C: Conversion Between Hg18 And Hg19
6.6 years ago by Malachi Griffith 19k
0
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0
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5.7k
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Comment: C: How Do You Manage Moving Existing Projects To A New Genome Build?
6.6 years ago by Malachi Griffith 19k
1
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0
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3.9k
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Comment: C: Visualizing genomic data: techniques and challenges. Our interview with Dr. Mala
6.7 years ago by Malachi Griffith 19k
0
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0
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4.7k
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Comment: C: Workshop: Genomic Data Visualization and Interpretation (Berlin, Germany)
6.7 years ago by Malachi Griffith 19k
0
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0
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15k
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Comment: C: Exploring cancer mutation data portals
7.0 years ago by Malachi Griffith 19k
1
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0
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44k
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Answer: C: Gene Fusion Detection: Rna-Seq Data
7.1 years ago by Malachi Griffith 19k
3
votes
3
replies
5.4k
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Running Tophat --Fusion-Search On A Filtered Bam That Was Generated By Tophat
tophat rna-seq
updated 7.2 years ago by 20 • written 11.6 years ago by 19k
0
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0
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71k
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Comment: C: Database Of Tumor Suppressors And/Or Oncogenes
7.3 years ago by Malachi Griffith 19k
3
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0
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5.3k
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Comment: C: CIViC - Clinical Interpretation of Variants in Cancer
7.5 years ago by Malachi Griffith 19k
0
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0
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2.1k
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Comment: C: What are the resources to design the most comprehensive clinical SNP chip?
7.6 years ago by Malachi Griffith 19k
1
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0
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2.9k
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Comment: C: Best way to obtain list of all drug-variant associations from CIViC
updated 7.6 years ago by 20k • written 7.6 years ago by 19k
0
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0
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15k
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Comment: C: How To Get Phasing Status From Vcf Files
7.7 years ago by Malachi Griffith 19k
1
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2
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5.6k
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Answer: A: PubChem CID data retrieval
7.9 years ago by Malachi Griffith 19k
0
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0
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3.2k
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Comment: C: Current Topics in Genome Analysis 2016 (collection of educational lectures)
7.9 years ago by Malachi Griffith 19k
0
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0
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8.5k
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Comment: C: Current Topics in Genome Analysis 2014 (collection of educational lectures)
7.9 years ago by Malachi Griffith 19k
0
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0
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8.5k
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Comment: C: Current Topics in Genome Analysis 2014 (collection of educational lectures)
7.9 years ago by Malachi Griffith 19k
15
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1
reply
3.2k
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Tutorial: Current Topics in Genome Analysis 2016 (collection of educational lectures)
genomics training lectures workshop
updated 12 months ago by 43k • written 7.9 years ago by 19k
3
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0
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2.9k
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Answer: A: Detecting a small set of given Intron-Exon junctions in a RNA-Seq dataset
8.0 years ago by Malachi Griffith 19k
3
votes
0
replies
5.4k
views
Answer: Answer: Finding Mutation Hotspot At Level Of Amino Acid By Spatial Proximity In Protein
updated 21 months ago by 43k • written 8.2 years ago by 19k
9
votes
0
replies
4.4k
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Tutorial: Analysis of dbGaP data on the cloud
AWS dbGaP Cloud
updated 21 months ago by 43k • written 8.2 years ago by 19k
3
votes
1
reply
45k
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Comment: C: Up-to-date Online RNA Sequence Analysis Training/Courses/Papers?
8.2 years ago by Malachi Griffith 19k
20
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4
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7.6k
views
Data Set Suitable For Comparing Wgs, Exome, And Rna-Seq Data Generated From The Same Samples
exome rna-seq data wgs
updated 2.0 years ago by 43k • written 11.2 years ago by 19k
0
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0
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8.9k
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Comment: C: Best Discordant Pair Structural Variant (Sv) Caller?
8.4 years ago by Malachi Griffith 19k
0
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0
replies
8.5k
views
Comment: C: Current Topics in Genome Analysis 2014 (collection of educational lectures)
8.4 years ago by Malachi Griffith 19k
0
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0
replies
26k
views
Comment: Comment: The New Grch38 Human Genome Browser Has Arrived!
updated 2.2 years ago by 43k • written 8.4 years ago by 19k
1
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0
replies
20k
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Comment: Comment: Publications for individualized medicine in cancer by whole genome, exome or tra
updated 19 months ago by 43k • written 8.6 years ago by 19k
1
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1
reply
20k
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Comment: Comment: Publications for individualized medicine in cancer by whole genome, exome or tra
updated 19 months ago by 43k • written 8.6 years ago by 19k
8
votes
0
replies
13k
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Answer: Answer: Which program, tool, or strategy do you use to visualize genomic rearrangements?
updated 2.5 years ago by 43k • written 8.6 years ago by 19k
105
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3
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62k
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Answer: Answer: Recommended Tools For Alternative Splicing Detection From Rna-Seq Data
updated 2.6 years ago by 43k • written 11.1 years ago by 19k
2
votes
1
reply
3.1k
views
Tool: Variationhunter
structural-variant sv
updated 19 months ago by 43k • written 11.8 years ago by 19k
474 results • Page 2 of 10
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