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0
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0
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908
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Comment: Comment: Overlapping bases count in WGS
2.5 years ago by NB ▴ 960
0
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0
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908
views
Comment: Comment: Overlapping bases count in WGS
2.5 years ago by NB ▴ 960
0
votes
4
replies
908
views
Overlapping bases count in WGS
wgs overlap count metrics bases
2.5 years ago by NB ▴ 960
12
votes
3
replies
20k
views
Calculate z-scores from GWAS summary stats
summary-stats GWAS z-scores
updated 21 months ago by 43k • written 9.0 years ago by ▴ 960
5
votes
11
replies
2.0k
views
CNV and pseudogenes
cnv NGS pseudogenes exomedepth
updated 3.9 years ago by ▴ 360 • written 5.6 years ago by ▴ 960
1
vote
6
replies
1.9k
views
Calculate coverage from SAM file
sam coverage no header samtools
updated 4.2 years ago by ▴ 330 • written 4.3 years ago by ▴ 960
0
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0
replies
1.9k
views
Comment: C: Calculate coverage from SAM file
4.3 years ago by NB ▴ 960
0
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0
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4.8k
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Comment: C: If the odds ratio of a SNP is < 1, does that mean the minor allele is protective
4.7 years ago by NB ▴ 960
2
votes
9
replies
3.8k
views
Convert vcf phased data to plink
vcf plink phased-haplotype
updated 9 months ago by 43k • written 4.8 years ago by ▴ 960
1
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0
replies
3.8k
views
Comment: C: Convert vcf phased data to plink
4.8 years ago by NB ▴ 960
0
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1
reply
3.8k
views
Comment: C: Convert vcf phased data to plink
4.8 years ago by NB ▴ 960
0
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1
reply
3.8k
views
Comment: C: Convert vcf phased data to plink
4.8 years ago by NB ▴ 960
0
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1
reply
3.8k
views
Comment: C: Convert vcf phased data to plink
4.8 years ago by NB ▴ 960
1
vote
1
reply
3.6k
views
Answer: C: hg19 interval list
5.0 years ago by NB ▴ 960
5
votes
8
replies
2.6k
views
Downsample BAM for targeted NGS panels
downsample targeted-NGS sambamba
updated 5.0 years ago by ▴ 30 • written 5.1 years ago by ▴ 960
1
vote
0
replies
2.3k
views
Comment: C: Identify or update refseq transcript version on snpeff
5.0 years ago by NB ▴ 960
0
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1
reply
3.2k
views
Plots using GWAS and eQTL datasets with locuszoom
GWAS eQTL locuszoom plots
updated 2.2 years ago by 43k • written 9.4 years ago by ▴ 960
0
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1
reply
1.9k
views
Comment: C: Approximately following the GATK recommended workflow for DNA sequence data, my
5.1 years ago by NB ▴ 960
4
votes
1
reply
13k
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Answer: A: How can I convert .ped file to bed+bim+fam file using plink 1.9?
5.1 years ago by NB ▴ 960
0
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3
replies
1.9k
views
Comment: C: Approximately following the GATK recommended workflow for DNA sequence data, my
5.1 years ago by NB ▴ 960
0
votes
1
reply
2.6k
views
Comment: C: Downsample BAM for targeted NGS panels
5.1 years ago by NB ▴ 960
0
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0
replies
2.6k
views
Comment: C: Downsample BAM for targeted NGS panels
5.1 years ago by NB ▴ 960
0
votes
1
reply
2.6k
views
Comment: C: Downsample BAM for targeted NGS panels
5.1 years ago by NB ▴ 960
0
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1
reply
4.5k
views
Comment: C: how to convert a list of genes to BED file?
5.2 years ago by NB ▴ 960
0
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1
reply
5.0k
views
Comment: C: How to extract SNPs from vcf file based on Population
5.2 years ago by NB ▴ 960
0
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1
reply
1.9k
views
Comment: C: File format for HGMD pro file flat
5.2 years ago by NB ▴ 960
0
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1
reply
1.9k
views
Comment: C: File format for HGMD pro file flat
5.2 years ago by NB ▴ 960
0
votes
1
reply
1.9k
views
Comment: C: File format for HGMD pro file flat
5.2 years ago by NB ▴ 960
0
votes
7
replies
1.9k
views
File format for HGMD pro file flat
variant-analysis HGMD annovar
updated 13 months ago by 43k • written 5.2 years ago by ▴ 960
3
votes
3
replies
1.6k
views
Extract info on OMIM Phenotype
OMIM database extract
updated 5.2 years ago by 141k • written 5.2 years ago by ▴ 960
0
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0
replies
1.6k
views
Comment: C: Extract info on OMIM Phenotype
5.2 years ago by NB ▴ 960
1
vote
1
reply
2.3k
views
Comment: C: GWAS data analysis strategy or pipeline
5.4 years ago by NB ▴ 960
1
vote
0
replies
1.5k
views
Comment: C: Alzheimer's disease and its classification
5.4 years ago by NB ▴ 960
2
votes
1
reply
1.5k
views
Comment: C: Alzheimer's disease and its classification
5.4 years ago by NB ▴ 960
0
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0
replies
3.0k
views
Comment: C: Difference in Haplotypecaller in GATKv4 Vs Gatk3.7
5.4 years ago by NB ▴ 960
2
votes
5
replies
3.0k
views
Difference in Haplotypecaller in GATKv4 Vs Gatk3.7
gatk haplotypecaller
updated 5.4 years ago by ▴ 90 • written 5.5 years ago by ▴ 960
0
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1
reply
3.0k
views
Comment: C: Difference in Haplotypecaller in GATKv4 Vs Gatk3.7
5.5 years ago by NB ▴ 960
1
vote
1
reply
2.0k
views
Comment: C: CNV and pseudogenes
5.6 years ago by NB ▴ 960
0
votes
1
reply
2.0k
views
Comment: C: CNV and pseudogenes
5.6 years ago by NB ▴ 960
0
votes
1
reply
2.0k
views
Comment: C: CNV and pseudogenes
5.6 years ago by NB ▴ 960
0
votes
0
replies
1.9k
views
Comment: C: Tools to detect CNV for NGS-mtDNA
5.6 years ago by NB ▴ 960
0
votes
1
reply
1.9k
views
Comment: C: Tools to detect CNV for NGS-mtDNA
5.6 years ago by NB ▴ 960
0
votes
4
replies
1.9k
views
Tools to detect CNV for NGS-mtDNA
mtDNA NGS
updated 10 months ago by 43k • written 5.6 years ago by ▴ 960
0
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1
reply
2.7k
views
Comment: C: Detection of deletion for mitochondrial NGS analysis at position 3107
5.6 years ago by NB ▴ 960
0
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0
replies
2.6k
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Comment: C: Next-Seq sequences map poorly to ref genome
5.7 years ago by NB ▴ 960
0
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1
reply
2.5k
views
Comment: C: Down sampling BAM files for CNV detection
5.7 years ago by NB ▴ 960
0
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1
reply
2.5k
views
Comment: C: Down sampling BAM files for CNV detection
5.7 years ago by NB ▴ 960
0
votes
1
reply
2.6k
views
Comment: C: Next-Seq sequences map poorly to ref genome
5.7 years ago by NB ▴ 960
8
votes
7
replies
2.5k
views
Down sampling BAM files for CNV detection
dowsampling BAM CNV NGS
updated 5.7 years ago by 47k • written 5.7 years ago by ▴ 960
0
votes
1
reply
2.6k
views
Comment: C: Next-Seq sequences map poorly to ref genome
5.7 years ago by NB ▴ 960
210 results • Page 1 of 5
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