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0
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0
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378
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Why ABSOLUTE calculate CCF=NA?
ABSOLUTE
21 months ago by Laven9 • 0
0
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0
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2.8k
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Comment: C: Which Driver-Gene Detecting Software Supports hg38?
23 months ago by Laven9 • 0
0
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0
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547
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Comment: C: error when running "SeuratToExpressionSet"
23 months ago by Laven9 • 0
0
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2
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547
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error when running "SeuratToExpressionSet"
SeuratToExpressionSet Seurat
23 months ago by Laven9 • 0
0
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1
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2.6k
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Comment: C: Set.seed in Seurat
2.2 years ago by Laven9 • 0
0
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4
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2.6k
views
Set.seed in Seurat
Seurat set.seed
updated 2.2 years ago by ▴ 890 • written 2.2 years ago by • 0
4
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3
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706
views
Strange plots I got from R studio
R
2.3 years ago by Laven9 • 0
0
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3
replies
1.8k
views
ERROR running annovar with cosmic90
annovar cosmic
updated 3.2 years ago by ▴ 30 • written 3.3 years ago by • 0
0
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0
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689
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How to interpret ABSOLUTE output?
ABSOLUTE
3.3 years ago by Laven9 • 0
0
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0
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1.7k
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Comment: A: A question on GetPileupSummaries (GATK)
3.3 years ago by Laven9 • 0
0
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2
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1.7k
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A question on GetPileupSummaries (GATK)
GetPileupSummaries
3.3 years ago by Laven9 • 0
0
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0
replies
2.4k
views
Comment: A: A question on GenomicsDBImport (GATK)
updated 3.4 years ago by 125k • written 3.4 years ago by • 0
0
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0
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2.4k
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Comment: A: A question on GenomicsDBImport (GATK)
3.4 years ago by Laven9 • 0
0
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4
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2.4k
views
A question on GenomicsDBImport (GATK)
GenomicsDBImport
3.4 years ago by Laven9 • 0
2
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3
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1.5k
views
Can Mutect2 be used for paper?
gatk Mutect2
updated 3.5 years ago by 10k • written 3.5 years ago by • 0
0
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0
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1.5k
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Comment: C: Can Mutect2 be used for paper?
3.5 years ago by Laven9 • 0
0
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0
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579
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Comment: C: What tools could be used for false positive filtering of somatic variants called
3.5 years ago by Laven9 • 0
0
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1
reply
579
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What tools could be used for false positive filtering of somatic variants called? And how do they work?
next-gen
updated 3.5 years ago by 15k • written 3.5 years ago by • 0
0
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0
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760
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Comment: C: A small detail when use VEP
3.5 years ago by Laven9 • 0
1
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2
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760
views
A small detail when use VEP
VEP
updated 3.5 years ago by 47k • written 3.5 years ago by • 0
0
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0
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1.3k
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Comment: C: How long will bam-readcount take to run human samples?
3.5 years ago by Laven9 • 0
0
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1
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1.3k
views
Comment: C: How long will bam-readcount take to run human samples?
3.5 years ago by Laven9 • 0
0
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1
reply
1.3k
views
Comment: C: How long will bam-readcount take to run human samples?
3.6 years ago by Laven9 • 0
1
vote
13
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1.3k
views
How long will bam-readcount take to run human samples?
bam-readcounts
updated 3.6 years ago by 68k • written 3.6 years ago by • 0
0
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0
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1.3k
views
Comment: C: How long will bam-readcount take to run human samples?
3.6 years ago by Laven9 • 0
0
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0
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1.3k
views
Comment: C: How long will bam-readcount take to run human samples?
3.6 years ago by Laven9 • 0
0
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1
reply
1.3k
views
Comment: C: How long will bam-readcount take to run human samples?
3.6 years ago by Laven9 • 0
0
votes
1
reply
1.3k
views
How to interpret the output of gatk?
gatk mutect2 vcf2maf
updated 3.6 years ago by ▴ 80 • written 3.6 years ago by • 0
0
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0
replies
539
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Comment: C: Is there any frequently-used signature database?
3.7 years ago by Laven9 • 0
0
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2
replies
539
views
Is there any frequently-used signature database?
signature human cancer
updated 3.7 years ago by 16k • written 3.7 years ago by • 0
0
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1
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2.2k
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Comment: C: CNVkit output problem: Is "log2" the same as "Seg_mean"? OR how can I get "Seg_m
3.8 years ago by Laven9 • 0
0
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10
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2.2k
views
CNVkit output problem: Is "log2" the same as "Seg_mean"? OR how can I get "Seg_mean" with "log2"?
CNV CNVkit Seg_mean
updated 3.8 years ago by ★ 2.8k • written 4.0 years ago by • 0
0
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1
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2.2k
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Comment: C: CNVkit output problem: Is "log2" the same as "Seg_mean"? OR how can I get "Seg_m
3.8 years ago by Laven9 • 0
0
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0
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554
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How can I check my title of reads added by BWA mem -R?
WES BWA
3.8 years ago by Laven9 • 0
0
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2
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2.2k
views
Comment: A: CNVkit output problem: Is "log2" the same as "Seg_mean"? OR how can I get "Seg_m
updated 3.8 years ago by 37k • written 4.0 years ago by • 0
0
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1
reply
1.1k
views
How to skip vep-annotating step for vcf2maf
Vcf2maf
3.9 years ago by Laven9 • 0
0
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0
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2.4k
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Comment: C: How can I split WES FASTQ file into sub-files for each chromosome ?
3.9 years ago by Laven9 • 0
0
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0
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2.4k
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Comment: A: How can I split WES FASTQ file into sub-files for each chromosome ?
3.9 years ago by Laven9 • 0
3
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10
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2.4k
views
How can I split WES FASTQ file into sub-files for each chromosome ?
WES split fastq chromosome
3.9 years ago by Laven9 • 0
0
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0
replies
2.4k
views
Comment: C: How can I split WES FASTQ file into sub-files for each chromosome ?
3.9 years ago by Laven9 • 0
0
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1
reply
2.4k
views
Comment: C: How can I split WES FASTQ file into sub-files for each chromosome ?
3.9 years ago by Laven9 • 0
0
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0
replies
2.4k
views
Comment: C: How can I split WES FASTQ file into sub-files for each chromosome ?
3.9 years ago by Laven9 • 0
0
votes
1
reply
2.4k
views
Comment: C: How can I split WES FASTQ file into sub-files for each chromosome ?
3.9 years ago by Laven9 • 0
0
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0
replies
2.2k
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Comment: C: CNVkit output problem: Is "log2" the same as "Seg_mean"? OR how can I get "Seg_m
4.0 years ago by Laven9 • 0
0
votes
2
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1.5k
views
How should I input CNV files and mutation files into R to run ABSOLUTE? Respectively or integrated?
ABSOLUTE
updated 4.1 years ago by 84k • written 4.1 years ago by • 0
45 results • Page 1 of 1
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