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Comment: C: Biopieces Is A Bioinformatic Framework Of Tools Easily Used And Easily Created.
11.5 years ago by Chris Miller 22k
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Comment: C: A Simple Question On Rna-Seq Terminology
11.5 years ago by Chris Miller 22k
6
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Answer: A: Deletions, Translocations And Cnv From Rna-Seq
11.5 years ago by Chris Miller 22k
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Comment: C: Publishing Bioinformatics Results
11.5 years ago by Chris Miller 22k
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6.2k
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Comment: C: Biostar Ads Are Now Live. Feedback And Comments Are Sought.
11.5 years ago by Chris Miller 22k
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Answer: A: Relationship Between Dp Score And Coverage Visualized By Igv
11.5 years ago by Chris Miller 22k
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Answer: A: What Tools For Highly Detailed Analysis Of Point Mutation On A Known Structure
11.5 years ago by Chris Miller 22k
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Comment: C: Bioinformatics And Cancer Genomics At The Genome Institute - Washington Universi
11.5 years ago by Chris Miller 22k
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9.3k
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Comment: C: Transition/Transversion Ratio From Fastq Files
11.5 years ago by Chris Miller 22k
3
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Answer: A: Transition/Transversion Ratio From Fastq Files
11.5 years ago by Chris Miller 22k
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Answer: A: Obtaining .Sqn Files For Wgs Submission At Ncbi ?
11.5 years ago by Chris Miller 22k
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Comment: C: Bioinformatics And Cancer Genomics At The Genome Institute - Washington Universi
11.5 years ago by Chris Miller 22k
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Job: Bioinformatics And Cancer Genomics At The Genome Institute - Washington University Stl
ngs cancer sequencing genomics
updated 21 months ago by 44k • written 11.5 years ago by 22k
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Comment: C: Which Snp Caller / Method To Use After Aligning Rna-Seq With Tophat
11.5 years ago by Chris Miller 22k
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4.2k
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Answer: A: Where To Find The Sequence Data About Leukemia?
11.5 years ago by Chris Miller 22k
4
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3.4k
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Answer: A: Genome Music Smg: How Can A Single Mutation Be Statistically Significant?
11.5 years ago by Chris Miller 22k
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1.8k
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Answer: A: Web Page Converting Seq Mapping Score
11.5 years ago by Chris Miller 22k
1
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4.4k
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Answer: A: 'Floating Point Exception' Error While Running Somaticsniper
11.5 years ago by Chris Miller 22k
3
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42k
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Comment: C: Will Python Take The Place Of R?
11.5 years ago by Chris Miller 22k
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12k
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Comment: C: Grab Coordinate Of Centromeres From Ucsc
11.5 years ago by Chris Miller 22k
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1
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12k
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Comment: C: Grab Coordinate Of Centromeres From Ucsc
11.5 years ago by Chris Miller 22k
4
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3.7k
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Answer: A: How Many Cells Will Be Involved In One Dna Or Rna Sequencing?
11.5 years ago by Chris Miller 22k
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Comment: C: Analysis Of Cnv
11.6 years ago by Chris Miller 22k
1
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4.9k
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Comment: C: Need Advice On How To Become A Senior Bioinformatician
11.6 years ago by Chris Miller 22k
2
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1
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16k
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Comment: C: What Is The Difference Between Structural Variants (Svs) And Copy-Number Variant
11.6 years ago by Chris Miller 22k
5
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4.9k
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Comment: C: Need Advice On How To Become A Senior Bioinformatician
11.6 years ago by Chris Miller 22k
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Answer: A: What Is The Difference Between Structural Variants (Svs) And Copy-Number Variant
11.6 years ago by Chris Miller 22k
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0
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18k
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Comment: C: Discrepancy In Samtools Mpileup/Depth And Bedtools Genomecoveragebed Counts
11.6 years ago by Chris Miller 22k
1
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1
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4.4k
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Answer: A: Which Snp Caller / Method To Use After Aligning Rna-Seq With Tophat
11.6 years ago by Chris Miller 22k
4
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3.3k
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Answer: A: Looking For Frequency Of A Very Specific Rna Editing Event In Publicly Available
11.6 years ago by Chris Miller 22k
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2
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5.1k
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Comment: C: Analysis Of Cnv
11.6 years ago by Chris Miller 22k
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Answer: A: Difference In Number Of Reads Using Samtools View And Igv
11.6 years ago by Chris Miller 22k
4
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5.3k
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Answer: A: Looking For Rna-Seq Data Sets Of Breast Cancer Or Liver Cancer.
11.6 years ago by Chris Miller 22k
0
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Comment: C: Recommendation For Cnv Calling Program Based On Depth Of Coverage From Bam
11.6 years ago by Chris Miller 22k
1
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1
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2.5k
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Answer: A: Is There A Way To Know When A Particular Tcga Sample Was Analyzed And Added To T
11.6 years ago by Chris Miller 22k
1
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1
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2.5k
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Comment: C: Is There A Way To Know When A Particular Tcga Sample Was Analyzed And Added To T
11.6 years ago by Chris Miller 22k
1
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1
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2.8k
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Answer: A: Music Calcroicovg Core Dump: "Floating Point Exception"
11.6 years ago by Chris Miller 22k
0
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2.3k
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Comment: C: How Many Differing Snv To Expect Between Two Cancer Samples With Identical Origi
11.6 years ago by Chris Miller 22k
1
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2.3k
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Answer: A: How Many Differing Snv To Expect Between Two Cancer Samples With Identical Origi
11.6 years ago by Chris Miller 22k
0
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0
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6.4k
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Comment: C: How To Fix A Bam-Readcount Sm Error: "Couldn'T Grab Single-End Mapping Quality F
11.6 years ago by Chris Miller 22k
1
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1
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6.4k
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Answer: A: How To Fix A Bam-Readcount Sm Error: "Couldn'T Grab Single-End Mapping Quality F
11.6 years ago by Chris Miller 22k
2
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0
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3.2k
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Answer: A: How To Determine Structural Variant Type Or Reformat Breakpoint Data To Bam
11.7 years ago by Chris Miller 22k
0
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0
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2.5k
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Comment: C: Needed Read Length To Solve Dna Fragments Containing Alu Elements In Vertebrate
11.7 years ago by Chris Miller 22k
0
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0
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4.8k
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Answer: A: Merging Segments From Varscan2 Output...
11.7 years ago by Chris Miller 22k
0
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0
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2.1k
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Answer: A: Running A Somatic Sniper With Marked Duplicate And Sorted Bam File.
11.7 years ago by Chris Miller 22k
2
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1
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2.8k
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Answer: A: Bam2Cfg Parameter Description
11.7 years ago by Chris Miller 22k
2
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1
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5.0k
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Answer: A: Whole Genome Dna Amplification Before Applying Wgs
11.7 years ago by Chris Miller 22k
0
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0
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4.9k
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Comment: C: Problems After Loading Varscan 2 Output Into Bioconductor.Dnacopy
11.7 years ago by Chris Miller 22k
0
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2
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4.9k
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Answer: A: Problems After Loading Varscan 2 Output Into Bioconductor.Dnacopy
11.7 years ago by Chris Miller 22k
0
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1
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7.2k
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Answer: A: Question About Mergesegment.Pl In Varscan 2
11.8 years ago by Chris Miller 22k
1,036 results • Page 15 of 21
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