Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
1
vote
2
replies
5.8k
views
Comment: C: Biopieces Is A Bioinformatic Framework Of Tools Easily Used And Easily Created.
12.4 years ago by Chris Miller 22k
2
votes
0
replies
5.2k
views
Comment: C: A Simple Question On Rna-Seq Terminology
12.4 years ago by Chris Miller 22k
6
votes
0
replies
4.6k
views
Answer: A: Deletions, Translocations And Cnv From Rna-Seq
12.4 years ago by Chris Miller 22k
1
vote
0
replies
6.7k
views
Comment: C: Publishing Bioinformatics Results
12.4 years ago by Chris Miller 22k
0
votes
2
replies
7.6k
views
Comment: C: Biostar Ads Are Now Live. Feedback And Comments Are Sought.
12.4 years ago by Chris Miller 22k
1
vote
1
reply
3.8k
views
Answer: A: Relationship Between Dp Score And Coverage Visualized By Igv
12.5 years ago by Chris Miller 22k
0
votes
0
replies
3.6k
views
Answer: A: What Tools For Highly Detailed Analysis Of Point Mutation On A Known Structure
12.5 years ago by Chris Miller 22k
0
votes
1
reply
5.2k
views
Comment: C: Bioinformatics And Cancer Genomics At The Genome Institute - Washington Universi
12.5 years ago by Chris Miller 22k
1
vote
1
reply
10k
views
Comment: C: Transition/Transversion Ratio From Fastq Files
12.5 years ago by Chris Miller 22k
3
votes
1
reply
10k
views
Answer: A: Transition/Transversion Ratio From Fastq Files
12.5 years ago by Chris Miller 22k
2
votes
0
replies
5.5k
views
Answer: A: Obtaining .Sqn Files For Wgs Submission At Ncbi ?
12.5 years ago by Chris Miller 22k
0
votes
0
replies
5.2k
views
Comment: C: Bioinformatics And Cancer Genomics At The Genome Institute - Washington Universi
12.5 years ago by Chris Miller 22k
9
votes
5
replies
5.2k
views
Job: Bioinformatics And Cancer Genomics At The Genome Institute - Washington University Stl
ngs cancer sequencing genomics
updated 2.7 years ago by 45k • written 12.5 years ago by 22k
0
votes
0
replies
4.9k
views
Comment: C: Which Snp Caller / Method To Use After Aligning Rna-Seq With Tophat
12.5 years ago by Chris Miller 22k
1
vote
1
reply
5.1k
views
Answer: A: Where To Find The Sequence Data About Leukemia?
12.5 years ago by Chris Miller 22k
4
votes
1
reply
3.6k
views
Answer: A: Genome Music Smg: How Can A Single Mutation Be Statistically Significant?
12.5 years ago by Chris Miller 22k
3
votes
0
replies
2.0k
views
Answer: A: Web Page Converting Seq Mapping Score
12.5 years ago by Chris Miller 22k
1
vote
1
reply
4.9k
views
Answer: A: 'Floating Point Exception' Error While Running Somaticsniper
12.5 years ago by Chris Miller 22k
3
votes
0
replies
46k
views
Comment: C: Will Python Take The Place Of R?
12.5 years ago by Chris Miller 22k
0
votes
0
replies
12k
views
Comment: C: Grab Coordinate Of Centromeres From Ucsc
12.5 years ago by Chris Miller 22k
0
votes
1
reply
12k
views
Comment: C: Grab Coordinate Of Centromeres From Ucsc
12.5 years ago by Chris Miller 22k
4
votes
1
reply
4.1k
views
Answer: A: How Many Cells Will Be Involved In One Dna Or Rna Sequencing?
12.5 years ago by Chris Miller 22k
0
votes
1
reply
6.0k
views
Comment: C: Analysis Of Cnv
12.5 years ago by Chris Miller 22k
1
vote
1
reply
5.8k
views
Comment: C: Need Advice On How To Become A Senior Bioinformatician
12.5 years ago by Chris Miller 22k
2
votes
1
reply
18k
views
Comment: C: What Is The Difference Between Structural Variants (Svs) And Copy-Number Variant
12.5 years ago by Chris Miller 22k
5
votes
1
reply
5.8k
views
Comment: C: Need Advice On How To Become A Senior Bioinformatician
12.5 years ago by Chris Miller 22k
8
votes
0
replies
18k
views
Answer: A: What Is The Difference Between Structural Variants (Svs) And Copy-Number Variant
12.5 years ago by Chris Miller 22k
0
votes
0
replies
20k
views
Comment: C: Discrepancy In Samtools Mpileup/Depth And Bedtools Genomecoveragebed Counts
12.5 years ago by Chris Miller 22k
1
vote
1
reply
4.9k
views
Answer: A: Which Snp Caller / Method To Use After Aligning Rna-Seq With Tophat
12.5 years ago by Chris Miller 22k
4
votes
0
replies
3.6k
views
Answer: A: Looking For Frequency Of A Very Specific Rna Editing Event In Publicly Available
12.5 years ago by Chris Miller 22k
0
votes
2
replies
6.0k
views
Comment: C: Analysis Of Cnv
12.5 years ago by Chris Miller 22k
0
votes
0
replies
5.5k
views
Answer: A: Difference In Number Of Reads Using Samtools View And Igv
12.5 years ago by Chris Miller 22k
4
votes
0
replies
5.7k
views
Answer: A: Looking For Rna-Seq Data Sets Of Breast Cancer Or Liver Cancer.
12.5 years ago by Chris Miller 22k
0
votes
0
replies
4.0k
views
Comment: C: Recommendation For Cnv Calling Program Based On Depth Of Coverage From Bam
12.6 years ago by Chris Miller 22k
1
vote
1
reply
2.9k
views
Answer: A: Is There A Way To Know When A Particular Tcga Sample Was Analyzed And Added To T
12.6 years ago by Chris Miller 22k
1
vote
1
reply
2.9k
views
Comment: C: Is There A Way To Know When A Particular Tcga Sample Was Analyzed And Added To T
12.6 years ago by Chris Miller 22k
1
vote
1
reply
3.1k
views
Answer: A: Music Calcroicovg Core Dump: "Floating Point Exception"
12.6 years ago by Chris Miller 22k
0
votes
0
replies
2.6k
views
Comment: C: How Many Differing Snv To Expect Between Two Cancer Samples With Identical Origi
12.6 years ago by Chris Miller 22k
1
vote
0
replies
2.6k
views
Answer: A: How Many Differing Snv To Expect Between Two Cancer Samples With Identical Origi
12.6 years ago by Chris Miller 22k
0
votes
0
replies
7.1k
views
Comment: C: How To Fix A Bam-Readcount Sm Error: "Couldn'T Grab Single-End Mapping Quality F
12.6 years ago by Chris Miller 22k
1
vote
1
reply
7.1k
views
Answer: A: How To Fix A Bam-Readcount Sm Error: "Couldn'T Grab Single-End Mapping Quality F
12.6 years ago by Chris Miller 22k
2
votes
0
replies
3.7k
views
Answer: A: How To Determine Structural Variant Type Or Reformat Breakpoint Data To Bam
12.6 years ago by Chris Miller 22k
0
votes
0
replies
2.9k
views
Comment: C: Needed Read Length To Solve Dna Fragments Containing Alu Elements In Vertebrate
12.7 years ago by Chris Miller 22k
0
votes
0
replies
5.5k
views
Answer: A: Merging Segments From Varscan2 Output...
12.7 years ago by Chris Miller 22k
0
votes
0
replies
2.3k
views
Answer: A: Running A Somatic Sniper With Marked Duplicate And Sorted Bam File.
12.7 years ago by Chris Miller 22k
2
votes
1
reply
3.2k
views
Answer: A: Bam2Cfg Parameter Description
12.7 years ago by Chris Miller 22k
2
votes
1
reply
5.9k
views
Answer: A: Whole Genome Dna Amplification Before Applying Wgs
12.7 years ago by Chris Miller 22k
0
votes
0
replies
5.6k
views
Comment: C: Problems After Loading Varscan 2 Output Into Bioconductor.Dnacopy
12.7 years ago by Chris Miller 22k
0
votes
2
replies
5.6k
views
Answer: A: Problems After Loading Varscan 2 Output Into Bioconductor.Dnacopy
12.7 years ago by Chris Miller 22k
0
votes
1
reply
8.0k
views
Answer: A: Question About Mergesegment.Pl In Varscan 2
12.7 years ago by Chris Miller 22k
1,036 results • Page 15 of 21
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6