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2
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1
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7.2k
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Comment: C: Middle author, but not first author projects. How would you approach this?
5.1 years ago by Chris Miller 22k
2
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2
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7.2k
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Comment: C: Middle author, but not first author projects. How would you approach this?
5.1 years ago by Chris Miller 22k
1
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5
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2.1k
views
Convert indel list with [-/A] notation to VCF with adjacent base
vcf faidx bed
updated 10 months ago by 43k • written 5.3 years ago by 22k
0
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0
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3.1k
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Comment: C: CNVkit: Choice of Bin Size and CNV Calling
5.2 years ago by Chris Miller 22k
2
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1
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3.1k
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Answer: A: CNVkit: Choice of Bin Size and CNV Calling
5.2 years ago by Chris Miller 22k
1
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0
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1.8k
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Job: Bioinformatics Developer/Analyst - Washington University in St. Louis
wustl
updated 11 months ago by 43k • written 5.2 years ago by 22k
0
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1
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2.8k
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Comment: C: Visualize VarScan2 Copy Number Aberrations in IGV
5.2 years ago by Chris Miller 22k
3
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0
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2.3k
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Answer: A: Reproducing this picture
5.3 years ago by Chris Miller 22k
0
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0
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1.5k
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Comment: C: Detecting known, low frequency SNPs in bacterial populations
5.3 years ago by Chris Miller 22k
1
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1
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1.5k
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Answer: A: Detecting known, low frequency SNPs in bacterial populations
5.3 years ago by Chris Miller 22k
1
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0
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1.3k
views
Answer: A: Does sciClone work on mouse exome data?
5.3 years ago by Chris Miller 22k
0
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0
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1.3k
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Answer: A: SciClone works with 1d clustering, but not 2d?
5.3 years ago by Chris Miller 22k
1
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0
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1.2k
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Answer: A: regions with very different VAF fall into one cluster
5.3 years ago by Chris Miller 22k
0
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0
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2.1k
views
Answer: A: Convert indel list with [-/A] notation to VCF with adjacent base
5.3 years ago by Chris Miller 22k
0
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0
replies
1.5k
views
Answer: A: Cancer Genomics and Bioinformatics positions at WashU (Griffith Lab)
5.4 years ago by Chris Miller 22k
0
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0
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1.6k
views
Answer: A: Postdoc position in single-cell cancer genomics
5.4 years ago by Chris Miller 22k
3
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1
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1.1k
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Comment: C: Finding SNV showing allele specific bias
5.4 years ago by Chris Miller 22k
18
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6
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9.9k
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Biomart Very Slow
biomart r
updated 5.4 years ago by ▴ 30 • written 13.9 years ago by 22k
1
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0
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1.2k
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Answer: A: Get Flanking Amino Acid Sequence
5.4 years ago by Chris Miller 22k
2
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0
replies
1.5k
views
Answer: A: Getting same SNPs both in cancer and normal files when seen in IGV - Integrativ
5.4 years ago by Chris Miller 22k
1
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0
replies
2.2k
views
Comment: C: a question about fishplot
5.5 years ago by Chris Miller 22k
1
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1
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2.2k
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Answer: A: a question about fishplot
5.5 years ago by Chris Miller 22k
1
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0
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4.5k
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Answer: A: How to load BAM files that do not have chromosome name in the header?
5.5 years ago by Chris Miller 22k
0
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0
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3.8k
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Comment: C: Where are mutation files (MAF) for TCGA normal samples on Firebrowse
5.6 years ago by Chris Miller 22k
1
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0
replies
4.7k
views
Answer: A: How can I find motifs under individual ATAC-peaks?
5.6 years ago by Chris Miller 22k
1
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1
reply
3.8k
views
Answer: A: Where are mutation files (MAF) for TCGA normal samples on Firebrowse
5.6 years ago by Chris Miller 22k
1
vote
1
reply
5.9k
views
Comment: C: Google announces DeepVariant
5.6 years ago by Chris Miller 22k
1
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0
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5.9k
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Comment: C: Google announces DeepVariant
5.6 years ago by Chris Miller 22k
1
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0
replies
3.6k
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Comment: C: SciClone on WES data
5.6 years ago by Chris Miller 22k
0
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0
replies
1.2k
views
Answer: A: Calling CNVs from WGS data
5.6 years ago by Chris Miller 22k
0
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1
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2.0k
views
Comment: C: bam2cfg.pl not able to find statistics : Breakdancer
5.6 years ago by Chris Miller 22k
27
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24
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2.5k
views
7 follow
Code Golf - bisulfite conversion
bisulfite bsseq code-golf
updated 11 months ago by 43k • written 5.6 years ago by 22k
0
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1
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2.5k
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Comment: C: Code Golf - bisulfite conversion
5.6 years ago by Chris Miller 22k
0
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0
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2.5k
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Comment: C: Code Golf - bisulfite conversion
5.6 years ago by Chris Miller 22k
0
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1
reply
2.5k
views
Comment: C: Code Golf - bisulfite conversion
5.6 years ago by Chris Miller 22k
2
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1
reply
2.9k
views
Answer: A: Running sciClone on cell prevalence (CP) data
updated 5.6 years ago by 43k • written 8.2 years ago by 22k
1
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0
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4.0k
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Comment: C: Fishplot R package
5.6 years ago by Chris Miller 22k
2
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0
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2.2k
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Answer: A: Is there a database which gives meta-level information of mutation(both nuclueot
updated 5.6 years ago by 43k • written 8.2 years ago by 22k
1
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0
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6.8k
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Answer: A: R phangorn phylogenetic analysis from somatic mutations' binary table
updated 5.6 years ago by 43k • written 8.2 years ago by 22k
0
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0
replies
1.8k
views
Answer: A: sciClone annotation file
updated 5.7 years ago by 43k • written 8.2 years ago by 22k
2
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1
reply
4.4k
views
Answer: A: Extracting Reads by position
updated 5.7 years ago by 43k • written 8.2 years ago by 22k
0
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2
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17k
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Answer: A: Writing Collaboration With Source-Control And Microsoft-Word
updated 5.7 years ago by 43k • written 13.8 years ago by 22k
1
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0
replies
2.8k
views
Answer: A: What Is The Statistical Framework To Compare Distribution Of Two Samples Of Geno
updated 5.7 years ago by 43k • written 13.8 years ago by 22k
1
vote
0
replies
12k
views
Answer: A: Statistics: Combinations In Python
updated 5.7 years ago by 43k • written 13.9 years ago by 22k
4
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0
replies
7.5k
views
Answer: A: How Can I Read The Contents Of Rdata!, Where Is It Located ? And How Can I Acces
updated 5.7 years ago by 43k • written 13.9 years ago by 22k
1
vote
0
replies
1.9k
views
Answer: A: Plotting Lines Of A Table In R
updated 5.7 years ago by 43k • written 14.0 years ago by 22k
3
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1
reply
8.4k
views
Answer: A: Rearranging Dna Sequences
updated 5.7 years ago by 43k • written 14.1 years ago by 22k
5
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4
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23k
views
Answer: Answer: How Do I Access And Query Entire Genome Sequences With R
updated 6 months ago by 43k • written 14.1 years ago by 22k
0
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0
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1.4k
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Comment: C: bam-readcount core dump
5.8 years ago by Chris Miller 22k
1
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0
replies
1.0k
views
Answer: A: high frequency SNPs (and other variations) after subtracting blood variants from
5.8 years ago by Chris Miller 22k
1,036 results • Page 3 of 21
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