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1
vote
1
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1.1k
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lofreq empty output?
lofreq
updated 2.3 years ago by ▴ 60 • written 4.0 years ago by ▴ 50
1
vote
4
replies
2.9k
views
Interpreting GISTIC2 output
GISTIC
updated 2.5 years ago by ★ 1.4k • written 3.6 years ago by ▴ 50
0
votes
2
replies
1.2k
views
HRD score LST?
cnv
updated 2.7 years ago by ★ 1.1k • written 3.6 years ago by ▴ 50
2
votes
1
reply
650
views
Getting sample IDs from dbGaP SRR?
dbgap
updated 3.2 years ago by 20 • written 3.3 years ago by ▴ 50
0
votes
0
replies
525
views
Extract VCF of tumor variants from a list of SNPs
mutect2 SNP
3.3 years ago by vctrm67 ▴ 50
0
votes
1
reply
2.2k
views
Comment: C: CNVKit for unmatched tumor-only WGS samples
3.3 years ago by vctrm67 ▴ 50
0
votes
6
replies
2.2k
views
CNVKit for unmatched tumor-only WGS samples
cnvkit
updated 14 months ago by ▴ 850 • written 3.3 years ago by ▴ 50
0
votes
1
reply
2.2k
views
Comment: C: CNVKit for unmatched tumor-only WGS samples
3.3 years ago by vctrm67 ▴ 50
0
votes
2
replies
1.1k
views
Mutect2 missing mutations
mutect
updated 3.4 years ago by 43k • written 3.4 years ago by ▴ 50
0
votes
0
replies
660
views
SV calling with duplication amplification
sv
3.5 years ago by vctrm67 ▴ 50
0
votes
1
reply
2.9k
views
Comment: C: Interpreting GISTIC2 output
3.6 years ago by vctrm67 ▴ 50
0
votes
1
reply
881
views
Comment: C: Amplification over deletion/Deletion over amplification?
3.6 years ago by vctrm67 ▴ 50
0
votes
3
replies
881
views
Amplification over deletion/Deletion over amplification?
gistic
updated 3.6 years ago by 87k • written 3.6 years ago by ▴ 50
5
votes
3
replies
3.1k
views
bedtools sort doesn't properly sort
bedtools
updated 3.6 years ago by 14k • written 3.7 years ago by ▴ 50
0
votes
0
replies
3.6k
views
Comment: C: GISTIC 2.0 markers
3.6 years ago by vctrm67 ▴ 50
0
votes
1
reply
3.6k
views
Comment: C: GISTIC 2.0 markers
3.6 years ago by vctrm67 ▴ 50
0
votes
0
replies
730
views
bedtools closest default?
bedtools
3.7 years ago by vctrm67 ▴ 50
0
votes
0
replies
3.7k
views
Comment: C: GISTIC 2.0 for sequencing data
3.7 years ago by vctrm67 ▴ 50
0
votes
1
reply
1.4k
views
Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
3.7 years ago by vctrm67 ▴ 50
0
votes
1
reply
1.4k
views
Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
3.7 years ago by vctrm67 ▴ 50
0
votes
1
reply
1.4k
views
Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
3.7 years ago by vctrm67 ▴ 50
0
votes
1
reply
1.4k
views
Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
3.7 years ago by vctrm67 ▴ 50
3
votes
9
replies
1.4k
views
Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
CNV
3.7 years ago by vctrm67 ▴ 50
0
votes
2
replies
3.7k
views
Comment: C: GISTIC 2.0 for sequencing data
3.7 years ago by vctrm67 ▴ 50
0
votes
1
reply
3.7k
views
Comment: C: GISTIC 2.0 for sequencing data
3.7 years ago by vctrm67 ▴ 50
0
votes
7
replies
3.7k
views
GISTIC 2.0 for sequencing data
gistic sequencing wgs cnv cna
3.7 years ago by vctrm67 ▴ 50
1
vote
3
replies
995
views
Calling CNVs using a single tumor sample
cnv
3.7 years ago by vctrm67 ▴ 50
0
votes
0
replies
510
views
CNV segmentation purpose
cnv
3.7 years ago by vctrm67 ▴ 50
1
vote
4
replies
803
views
Detecting aneuploidy in sequencing data or copy number profile?
ngs
updated 3.7 years ago by 13k • written 3.7 years ago by ▴ 50
0
votes
0
replies
803
views
Comment: A: Detecting aneuploidy in sequencing data or copy number profile?
3.7 years ago by vctrm67 ▴ 50
0
votes
0
replies
803
views
Comment: C: Detecting aneuploidy in sequencing data or copy number profile?
3.7 years ago by vctrm67 ▴ 50
0
votes
0
replies
594
views
ASCAT CN vs SNP probes
ascat
3.8 years ago by vctrm67 ▴ 50
0
votes
3
replies
2.2k
views
Calculating HRD score
HRD
updated 2.5 years ago by • 0 • written 3.8 years ago by ▴ 50
0
votes
1
reply
897
views
Number of probes per segment from ASCAT SNP array output?
ascat
3.8 years ago by vctrm67 ▴ 50
0
votes
0
replies
1.5k
views
Comment: C: TCGA CNV data reformatting
3.8 years ago by vctrm67 ▴ 50
0
votes
4
replies
1.5k
views
TCGA CNV data reformatting
CNV
updated 3.8 years ago by ▴ 550 • written 3.8 years ago by ▴ 50
0
votes
0
replies
1.5k
views
Comment: C: TCGA CNV data reformatting
3.8 years ago by vctrm67 ▴ 50
0
votes
1
reply
855
views
bcftools isec question?
bcftools
updated 3.9 years ago by 161k • written 3.9 years ago by ▴ 50
0
votes
2
replies
2.4k
views
Comment: C: Get nonoverlapping regions of two bed files
3.9 years ago by vctrm67 ▴ 50
0
votes
5
replies
2.4k
views
Get nonoverlapping regions of two bed files
bed
3.9 years ago by vctrm67 ▴ 50
1
vote
5
replies
1.6k
views
Calling CNVs without a normal
CNV
updated 4.0 years ago by 20 • written 4.3 years ago by ▴ 50
0
votes
1
reply
1.3k
views
Comment: C: Parallelizing GATK4 tools
4.0 years ago by vctrm67 ▴ 50
0
votes
1
reply
1.3k
views
Comment: C: Parallelizing GATK4 tools
4.0 years ago by vctrm67 ▴ 50
0
votes
0
replies
1.3k
views
Comment: C: Parallelizing GATK4 tools
4.0 years ago by vctrm67 ▴ 50
1
vote
7
replies
1.3k
views
Parallelizing GATK4 tools
GATK
4.0 years ago by vctrm67 ▴ 50
0
votes
1
reply
731
views
Rename "SM" tag in read group only
GATK
updated 2.8 years ago by ▴ 140 • written 4.1 years ago by ▴ 50
0
votes
0
replies
1.3k
views
Calling germline SNPs using GATK HaplotypeCaller in a single sample
GATK
4.1 years ago by vctrm67 ▴ 50
0
votes
1
reply
1.4k
views
Comment: C: Get intersection of files occuring in at least 2 files?
4.1 years ago by vctrm67 ▴ 50
0
votes
1
reply
1.4k
views
Comment: C: Get intersection of files occuring in at least 2 files?
4.1 years ago by vctrm67 ▴ 50
0
votes
1
reply
551
views
Why are BED files necessary for somatic calling?
somatic
4.2 years ago by vctrm67 ▴ 50
115 results • Page 1 of 3
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