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Comment: Comment: Overlapping bases count in WGS
4.0 years ago by NB ▴ 960
0
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0
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1.5k
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Comment: Comment: Overlapping bases count in WGS
4.0 years ago by NB ▴ 960
0
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4
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1.5k
views
Overlapping bases count in WGS
wgs overlap count metrics bases
4.0 years ago by NB ▴ 960
12
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3
replies
21k
views
Calculate z-scores from GWAS summary stats
summary-stats GWAS z-scores
updated 3.3 years ago by 45k • written 10.5 years ago by ▴ 960
5
votes
11
replies
3.0k
views
CNV and pseudogenes
cnv NGS pseudogenes exomedepth
updated 5.5 years ago by ▴ 400 • written 7.1 years ago by ▴ 960
1
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6
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2.5k
views
Calculate coverage from SAM file
sam coverage no header samtools
updated 5.8 years ago by ▴ 330 • written 5.8 years ago by ▴ 960
0
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0
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2.5k
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Comment: C: Calculate coverage from SAM file
5.8 years ago by NB ▴ 960
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0
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5.8k
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Comment: C: If the odds ratio of a SNP is < 1, does that mean the minor allele is protective
6.3 years ago by NB ▴ 960
2
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9
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5.0k
views
Convert vcf phased data to plink
vcf plink phased-haplotype
updated 2.3 years ago by 45k • written 6.3 years ago by ▴ 960
1
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0
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5.0k
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Comment: C: Convert vcf phased data to plink
6.3 years ago by NB ▴ 960
0
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1
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5.0k
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Comment: C: Convert vcf phased data to plink
6.3 years ago by NB ▴ 960
0
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1
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5.0k
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Comment: C: Convert vcf phased data to plink
6.3 years ago by NB ▴ 960
0
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1
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5.0k
views
Comment: C: Convert vcf phased data to plink
6.3 years ago by NB ▴ 960
1
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1
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4.8k
views
Answer: C: hg19 interval list
6.5 years ago by NB ▴ 960
5
votes
8
replies
3.8k
views
Downsample BAM for targeted NGS panels
downsample targeted-NGS sambamba
updated 6.5 years ago by ▴ 30 • written 6.6 years ago by ▴ 960
1
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0
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2.9k
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Comment: C: Identify or update refseq transcript version on snpeff
6.5 years ago by NB ▴ 960
0
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1
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3.7k
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Plots using GWAS and eQTL datasets with locuszoom
GWAS eQTL locuszoom plots
updated 3.7 years ago by 45k • written 11.0 years ago by ▴ 960
0
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1
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3.0k
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Comment: C: Approximately following the GATK recommended workflow for DNA sequence data, my
6.6 years ago by NB ▴ 960
4
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1
reply
16k
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Answer: A: How can I convert .ped file to bed+bim+fam file using plink 1.9?
6.6 years ago by NB ▴ 960
0
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3
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3.0k
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Comment: C: Approximately following the GATK recommended workflow for DNA sequence data, my
6.6 years ago by NB ▴ 960
0
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1
reply
3.8k
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Comment: C: Downsample BAM for targeted NGS panels
6.6 years ago by NB ▴ 960
0
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0
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3.8k
views
Comment: C: Downsample BAM for targeted NGS panels
6.6 years ago by NB ▴ 960
0
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1
reply
3.8k
views
Comment: C: Downsample BAM for targeted NGS panels
6.6 years ago by NB ▴ 960
0
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1
reply
5.1k
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Comment: C: how to convert a list of genes to BED file?
6.7 years ago by NB ▴ 960
0
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1
reply
5.8k
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Comment: C: How to extract SNPs from vcf file based on Population
6.7 years ago by NB ▴ 960
0
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1
reply
2.6k
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Comment: C: File format for HGMD pro file flat
6.8 years ago by NB ▴ 960
0
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1
reply
2.6k
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Comment: C: File format for HGMD pro file flat
6.8 years ago by NB ▴ 960
0
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1
reply
2.6k
views
Comment: C: File format for HGMD pro file flat
6.8 years ago by NB ▴ 960
0
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7
replies
2.6k
views
File format for HGMD pro file flat
variant-analysis HGMD annovar
updated 2.6 years ago by 45k • written 6.8 years ago by ▴ 960
3
votes
3
replies
2.1k
views
Extract info on OMIM Phenotype
OMIM database extract
updated 6.8 years ago by 154k • written 6.8 years ago by ▴ 960
0
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0
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2.1k
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Comment: C: Extract info on OMIM Phenotype
6.8 years ago by NB ▴ 960
1
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1
reply
3.2k
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Comment: C: GWAS data analysis strategy or pipeline
7.0 years ago by NB ▴ 960
1
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0
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2.4k
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Comment: C: Alzheimer's disease and its classification
7.0 years ago by NB ▴ 960
2
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1
reply
2.4k
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Comment: C: Alzheimer's disease and its classification
7.0 years ago by NB ▴ 960
0
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0
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3.9k
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Comment: C: Difference in Haplotypecaller in GATKv4 Vs Gatk3.7
7.0 years ago by NB ▴ 960
2
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5
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3.9k
views
Difference in Haplotypecaller in GATKv4 Vs Gatk3.7
gatk haplotypecaller
updated 7.0 years ago by ▴ 90 • written 7.0 years ago by ▴ 960
0
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1
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3.9k
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Comment: C: Difference in Haplotypecaller in GATKv4 Vs Gatk3.7
7.0 years ago by NB ▴ 960
1
vote
1
reply
3.0k
views
Comment: C: CNV and pseudogenes
7.1 years ago by NB ▴ 960
0
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1
reply
3.0k
views
Comment: C: CNV and pseudogenes
7.1 years ago by NB ▴ 960
0
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1
reply
3.0k
views
Comment: C: CNV and pseudogenes
7.1 years ago by NB ▴ 960
0
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0
replies
2.4k
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Comment: C: Tools to detect CNV for NGS-mtDNA
7.1 years ago by NB ▴ 960
0
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1
reply
2.4k
views
Comment: C: Tools to detect CNV for NGS-mtDNA
7.1 years ago by NB ▴ 960
0
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4
replies
2.4k
views
Tools to detect CNV for NGS-mtDNA
mtDNA NGS
updated 2.4 years ago by 45k • written 7.1 years ago by ▴ 960
0
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1
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3.8k
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Comment: C: Detection of deletion for mitochondrial NGS analysis at position 3107
7.2 years ago by NB ▴ 960
0
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0
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3.7k
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Comment: C: Next-Seq sequences map poorly to ref genome
7.2 years ago by NB ▴ 960
0
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1
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3.4k
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Comment: C: Down sampling BAM files for CNV detection
7.2 years ago by NB ▴ 960
0
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1
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3.4k
views
Comment: C: Down sampling BAM files for CNV detection
7.2 years ago by NB ▴ 960
0
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1
reply
3.7k
views
Comment: C: Next-Seq sequences map poorly to ref genome
7.2 years ago by NB ▴ 960
8
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7
replies
3.4k
views
Down sampling BAM files for CNV detection
dowsampling BAM CNV NGS
updated 7.2 years ago by 48k • written 7.2 years ago by ▴ 960
0
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1
reply
3.7k
views
Comment: C: Next-Seq sequences map poorly to ref genome
7.2 years ago by NB ▴ 960
210 results • Page 1 of 5
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