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Comment: Comment: Overlapping bases count in WGS
3.1 years ago by NB ▴ 960
0
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0
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1.1k
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Comment: Comment: Overlapping bases count in WGS
3.1 years ago by NB ▴ 960
0
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4
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1.1k
views
Overlapping bases count in WGS
wgs overlap count metrics bases
3.1 years ago by NB ▴ 960
12
votes
3
replies
20k
views
Calculate z-scores from GWAS summary stats
summary-stats GWAS z-scores
updated 2.4 years ago by 44k • written 9.6 years ago by ▴ 960
5
votes
11
replies
2.2k
views
CNV and pseudogenes
cnv NGS pseudogenes exomedepth
updated 4.5 years ago by ▴ 390 • written 6.2 years ago by ▴ 960
1
vote
6
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2.1k
views
Calculate coverage from SAM file
sam coverage no header samtools
updated 4.8 years ago by ▴ 330 • written 4.9 years ago by ▴ 960
0
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0
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2.1k
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Comment: C: Calculate coverage from SAM file
4.9 years ago by NB ▴ 960
0
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0
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5.1k
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Comment: C: If the odds ratio of a SNP is < 1, does that mean the minor allele is protective
5.3 years ago by NB ▴ 960
2
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9
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4.2k
views
Convert vcf phased data to plink
vcf plink phased-haplotype
updated 16 months ago by 44k • written 5.4 years ago by ▴ 960
1
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0
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4.2k
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Comment: C: Convert vcf phased data to plink
5.4 years ago by NB ▴ 960
0
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1
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4.2k
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Comment: C: Convert vcf phased data to plink
5.4 years ago by NB ▴ 960
0
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1
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4.2k
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Comment: C: Convert vcf phased data to plink
5.4 years ago by NB ▴ 960
0
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1
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4.2k
views
Comment: C: Convert vcf phased data to plink
5.4 years ago by NB ▴ 960
1
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1
reply
4.0k
views
Answer: C: hg19 interval list
5.6 years ago by NB ▴ 960
5
votes
8
replies
2.9k
views
Downsample BAM for targeted NGS panels
downsample targeted-NGS sambamba
updated 5.6 years ago by ▴ 30 • written 5.7 years ago by ▴ 960
1
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0
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2.5k
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Comment: C: Identify or update refseq transcript version on snpeff
5.6 years ago by NB ▴ 960
0
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1
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3.3k
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Plots using GWAS and eQTL datasets with locuszoom
GWAS eQTL locuszoom plots
updated 2.8 years ago by 44k • written 10.0 years ago by ▴ 960
0
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1
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2.2k
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Comment: C: Approximately following the GATK recommended workflow for DNA sequence data, my
5.7 years ago by NB ▴ 960
4
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1
reply
14k
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Answer: A: How can I convert .ped file to bed+bim+fam file using plink 1.9?
5.7 years ago by NB ▴ 960
0
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3
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2.2k
views
Comment: C: Approximately following the GATK recommended workflow for DNA sequence data, my
5.7 years ago by NB ▴ 960
0
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1
reply
2.9k
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Comment: C: Downsample BAM for targeted NGS panels
5.7 years ago by NB ▴ 960
0
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0
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2.9k
views
Comment: C: Downsample BAM for targeted NGS panels
5.7 years ago by NB ▴ 960
0
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1
reply
2.9k
views
Comment: C: Downsample BAM for targeted NGS panels
5.7 years ago by NB ▴ 960
0
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1
reply
4.7k
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Comment: C: how to convert a list of genes to BED file?
5.8 years ago by NB ▴ 960
0
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1
reply
5.2k
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Comment: C: How to extract SNPs from vcf file based on Population
5.8 years ago by NB ▴ 960
0
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1
reply
2.1k
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Comment: C: File format for HGMD pro file flat
5.8 years ago by NB ▴ 960
0
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1
reply
2.1k
views
Comment: C: File format for HGMD pro file flat
5.8 years ago by NB ▴ 960
0
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1
reply
2.1k
views
Comment: C: File format for HGMD pro file flat
5.8 years ago by NB ▴ 960
0
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7
replies
2.1k
views
File format for HGMD pro file flat
variant-analysis HGMD annovar
updated 20 months ago by 44k • written 5.8 years ago by ▴ 960
3
votes
3
replies
1.7k
views
Extract info on OMIM Phenotype
OMIM database extract
updated 5.8 years ago by 147k • written 5.8 years ago by ▴ 960
0
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0
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1.7k
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Comment: C: Extract info on OMIM Phenotype
5.8 years ago by NB ▴ 960
1
vote
1
reply
2.6k
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Comment: C: GWAS data analysis strategy or pipeline
6.0 years ago by NB ▴ 960
1
vote
0
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1.8k
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Comment: C: Alzheimer's disease and its classification
6.0 years ago by NB ▴ 960
2
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1
reply
1.8k
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Comment: C: Alzheimer's disease and its classification
6.0 years ago by NB ▴ 960
0
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0
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3.3k
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Comment: C: Difference in Haplotypecaller in GATKv4 Vs Gatk3.7
6.0 years ago by NB ▴ 960
2
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5
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3.3k
views
Difference in Haplotypecaller in GATKv4 Vs Gatk3.7
gatk haplotypecaller
updated 6.0 years ago by ▴ 90 • written 6.1 years ago by ▴ 960
0
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1
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3.3k
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Comment: C: Difference in Haplotypecaller in GATKv4 Vs Gatk3.7
6.1 years ago by NB ▴ 960
1
vote
1
reply
2.2k
views
Comment: C: CNV and pseudogenes
6.2 years ago by NB ▴ 960
0
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1
reply
2.2k
views
Comment: C: CNV and pseudogenes
6.2 years ago by NB ▴ 960
0
votes
1
reply
2.2k
views
Comment: C: CNV and pseudogenes
6.2 years ago by NB ▴ 960
0
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0
replies
2.1k
views
Comment: C: Tools to detect CNV for NGS-mtDNA
6.2 years ago by NB ▴ 960
0
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1
reply
2.1k
views
Comment: C: Tools to detect CNV for NGS-mtDNA
6.2 years ago by NB ▴ 960
0
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4
replies
2.1k
views
Tools to detect CNV for NGS-mtDNA
mtDNA NGS
updated 17 months ago by 44k • written 6.2 years ago by ▴ 960
0
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1
reply
3.0k
views
Comment: C: Detection of deletion for mitochondrial NGS analysis at position 3107
6.2 years ago by NB ▴ 960
0
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0
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2.9k
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Comment: C: Next-Seq sequences map poorly to ref genome
6.3 years ago by NB ▴ 960
0
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1
reply
2.8k
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Comment: C: Down sampling BAM files for CNV detection
6.3 years ago by NB ▴ 960
0
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1
reply
2.8k
views
Comment: C: Down sampling BAM files for CNV detection
6.3 years ago by NB ▴ 960
0
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1
reply
2.9k
views
Comment: C: Next-Seq sequences map poorly to ref genome
6.3 years ago by NB ▴ 960
8
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7
replies
2.8k
views
Down sampling BAM files for CNV detection
dowsampling BAM CNV NGS
updated 6.3 years ago by 47k • written 6.3 years ago by ▴ 960
0
votes
1
reply
2.9k
views
Comment: C: Next-Seq sequences map poorly to ref genome
6.3 years ago by NB ▴ 960
210 results • Page 1 of 5
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