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replies
3.7k
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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
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
views
Comment:
C: Google announces DeepVariant
5.6 years ago by
Chris Miller
22k
1
vote
0
replies
3.6k
views
Comment:
C: SciClone on WES data
5.6 years ago by
Chris Miller
22k
0
votes
1
reply
2.0k
views
Comment:
C: bam2cfg.pl not able to find statistics : Breakdancer
5.6 years ago by
Chris Miller
22k
0
votes
1
reply
2.4k
views
Comment:
C: Code Golf - bisulfite conversion
5.6 years ago by
Chris Miller
22k
0
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0
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2.4k
views
Comment:
C: Code Golf - bisulfite conversion
5.6 years ago by
Chris Miller
22k
0
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1
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2.4k
views
Comment:
C: Code Golf - bisulfite conversion
5.6 years ago by
Chris Miller
22k
1
vote
0
replies
4.0k
views
Comment:
C: Fishplot R package
5.6 years ago by
Chris Miller
22k
0
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0
replies
1.4k
views
Comment:
C: bam-readcount core dump
5.7 years ago by
Chris Miller
22k
0
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1
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8.8k
views
Comment:
C: Work With Dnacopy (Bioconductor) And Varscan Copynumber Results
5.9 years ago by
Chris Miller
22k
0
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0
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2.0k
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Comment:
C: Sciclone took too long
5.9 years ago by
Chris Miller
22k
1
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0
replies
1.9k
views
Comment:
C: SciClone: Why cluster in non-CN neutral region considering it infers only on CN
5.9 years ago by
Chris Miller
22k
0
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0
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3.3k
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Comment:
C: SciClone not numeric error
5.9 years ago by
Chris Miller
22k
0
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0
replies
3.1k
views
Comment:
C: Recreate reference fasta from bam file
6.0 years ago by
Chris Miller
22k
0
votes
0
replies
3.1k
views
Comment:
C: Recreate reference fasta from bam file
6.0 years ago by
Chris Miller
22k
0
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1
reply
3.1k
views
Comment:
C: Recreate reference fasta from bam file
6.0 years ago by
Chris Miller
22k
0
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1
reply
1.2k
views
Comment:
C: normalization when calling CNV areas on a genome-wide scale in tumor-germline sa
6.0 years ago by
Chris Miller
22k
0
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1
reply
1.2k
views
Comment:
C: normalization when calling CNV areas on a genome-wide scale in tumor-germline sa
6.0 years ago by
Chris Miller
22k
4
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0
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2.9k
views
Comment:
A: separate one column in two column R
6.0 years ago by
Chris Miller
22k
1
vote
1
reply
1.6k
views
Comment:
C: Bam to BigWig loss of data at MACS peaks (nothing in the BigWig why?)
6.1 years ago by
Chris Miller
22k
1
vote
0
replies
25k
views
Comment:
C: Difference Between Somatic And Germline Variant Calling?
6.1 years ago by
Chris Miller
22k
0
votes
0
replies
2.3k
views
Comment:
C: WGS coverage (depth) for CNV detection
6.2 years ago by
Chris Miller
22k
0
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1
reply
4.6k
views
Comment:
C: Problems After Loading Varscan 2 Output Into Bioconductor.Dnacopy
6.2 years ago by
Chris Miller
22k
1
vote
1
reply
1.9k
views
Comment:
C: Computer logistics of comparing genomes within same individual
6.2 years ago by
Chris Miller
22k
0
votes
1
reply
3.0k
views
Comment:
C: tumor/normal WGS with CNVkit has many small segments with small copy number chan
6.3 years ago by
Chris Miller
22k
1
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0
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15k
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Comment:
C: Number of Threads for BWA MEM
6.3 years ago by
Chris Miller
22k
1
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0
replies
2.3k
views
Comment:
C: N in fastq data
6.3 years ago by
Chris Miller
22k
0
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0
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4.0k
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Comment:
C: How to do DMR analysis with BiSeq (for RRBS methylation data)?
6.3 years ago by
Chris Miller
22k
0
votes
0
replies
11k
views
Comment:
C: Memory-Efficient Way To Transpose Csv/Text File?
6.3 years ago by
Chris Miller
22k
0
votes
0
replies
2.2k
views
Comment:
C: pipeline for neo-antigen identification
6.3 years ago by
Chris Miller
22k
0
votes
1
reply
2.2k
views
Comment:
C: pipeline for neo-antigen identification
6.3 years ago by
Chris Miller
22k
1
vote
1
reply
3.2k
views
Comment:
C: VarScan-Somatic Copy Number Alteration (CNA) Calling
6.4 years ago by
Chris Miller
22k
1
vote
0
replies
6.4k
views
Comment:
C: Bioinformatic or bioinformatics?
6.4 years ago by
Chris Miller
22k
1
vote
1
reply
3.2k
views
Comment:
C: VarScan-Somatic Copy Number Alteration (CNA) Calling
6.4 years ago by
Chris Miller
22k
2
votes
1
reply
5.9k
views
Comment:
C: Google announces DeepVariant
6.4 years ago by
Chris Miller
22k
1
vote
0
replies
1.3k
views
Comment:
C: PostDoc at Human Genome Sequencing Center at Baylor College of Medicine
6.4 years ago by
Chris Miller
22k
0
votes
1
reply
5.9k
views
Comment:
C: Google announces DeepVariant
6.4 years ago by
Chris Miller
22k
1
vote
1
reply
2.1k
views
Comment:
C: TCGA both blood and tissue for germline calling
6.4 years ago by
Chris Miller
22k
0
votes
0
replies
7.0k
views
Comment:
C: Bias During Exome Capture For Cnv Analysis
6.5 years ago by
Chris Miller
22k
1
vote
1
reply
2.7k
views
Comment:
C: NGS on cancer tumor
6.5 years ago by
Chris Miller
22k
0
votes
0
replies
2.7k
views
Comment:
C: NGS on cancer tumor
6.5 years ago by
Chris Miller
22k
0
votes
2
replies
2.7k
views
Comment:
C: NGS on cancer tumor
6.5 years ago by
Chris Miller
22k
4
votes
2
replies
4.1k
views
Comment:
C: Survey/Vote: If you could double the speed of any three commandline tools, which
6.5 years ago by
Chris Miller
22k
0
votes
0
replies
1.7k
views
Comment:
C: WGS data for healthy human women sequenced on Illumina HiSeq 2000?
6.6 years ago by
Chris Miller
22k
0
votes
1
reply
2.0k
views
Comment:
C: pindel not picking up on a lab-made gene knockout deletion
6.6 years ago by
Chris Miller
22k
1
vote
0
replies
4.6k
views
Comment:
C: Concept of Matched normal vs. Virtual Normal
6.6 years ago by
Chris Miller
22k
1
vote
0
replies
10k
views
Comment:
C: CNV detection from RNA-seq data
6.6 years ago by
Chris Miller
22k
1
vote
0
replies
2.1k
views
Comment:
C: sciClone input LOH
6.6 years ago by
Chris Miller
22k
0
votes
0
replies
3.5k
views
Comment:
C: How realible samtools/ bam-readcount /igvtools /pysamstats for finding deletions
6.6 years ago by
Chris Miller
22k
530 results • Page
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