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comments
0
votes
0
replies
1.0k
views
Comment:
Comment: Overlapping bases count in WGS
2.9 years ago by
NB
▴ 960
0
votes
0
replies
1.0k
views
Comment:
Comment: Overlapping bases count in WGS
2.9 years ago by
NB
▴ 960
0
votes
4
replies
1.0k
views
Overlapping bases count in WGS
wgs
overlap
count
metrics
bases
2.9 years ago by
NB
▴ 960
12
votes
3
replies
20k
views
Calculate z-scores from GWAS summary stats
summary-stats
GWAS
z-scores
updated 2.3 years ago by
Ram
44k • written 9.5 years ago by
NB
▴ 960
5
votes
11
replies
2.2k
views
CNV and pseudogenes
cnv
NGS
pseudogenes
exomedepth
updated 4.4 years ago by
geocarvalho
▴ 370 • written 6.1 years ago by
NB
▴ 960
1
vote
6
replies
2.1k
views
Calculate coverage from SAM file
sam
coverage
no header
samtools
updated 4.7 years ago by
onestop_data
▴ 330 • written 4.7 years ago by
NB
▴ 960
0
votes
0
replies
2.1k
views
Comment:
C: Calculate coverage from SAM file
4.7 years ago by
NB
▴ 960
0
votes
0
replies
5.1k
views
Comment:
C: If the odds ratio of a SNP is < 1, does that mean the minor allele is protective
5.2 years ago by
NB
▴ 960
2
votes
9
replies
4.2k
views
Convert vcf phased data to plink
vcf
plink
phased-haplotype
updated 15 months ago by
Ram
44k • written 5.3 years ago by
NB
▴ 960
1
vote
0
replies
4.2k
views
Comment:
C: Convert vcf phased data to plink
5.3 years ago by
NB
▴ 960
0
votes
1
reply
4.2k
views
Comment:
C: Convert vcf phased data to plink
5.3 years ago by
NB
▴ 960
0
votes
1
reply
4.2k
views
Comment:
C: Convert vcf phased data to plink
5.3 years ago by
NB
▴ 960
0
votes
1
reply
4.2k
views
Comment:
C: Convert vcf phased data to plink
5.3 years ago by
NB
▴ 960
1
vote
1
reply
3.9k
views
Answer:
C: hg19 interval list
5.4 years ago by
NB
▴ 960
5
votes
8
replies
2.9k
views
Downsample BAM for targeted NGS panels
downsample
targeted-NGS
sambamba
updated 5.5 years ago by
shrirambhosle
▴ 30 • written 5.6 years ago by
NB
▴ 960
1
vote
0
replies
2.5k
views
Comment:
C: Identify or update refseq transcript version on snpeff
5.5 years ago by
NB
▴ 960
0
votes
1
reply
3.3k
views
Plots using GWAS and eQTL datasets with locuszoom
GWAS
eQTL
locuszoom
plots
updated 2.6 years ago by
Ram
44k • written 9.9 years ago by
NB
▴ 960
0
votes
1
reply
2.2k
views
Comment:
C: Approximately following the GATK recommended workflow for DNA sequence data, my
5.6 years ago by
NB
▴ 960
4
votes
1
reply
14k
views
Answer:
A: How can I convert .ped file to bed+bim+fam file using plink 1.9?
5.6 years ago by
NB
▴ 960
0
votes
3
replies
2.2k
views
Comment:
C: Approximately following the GATK recommended workflow for DNA sequence data, my
5.6 years ago by
NB
▴ 960
0
votes
1
reply
2.9k
views
Comment:
C: Downsample BAM for targeted NGS panels
5.6 years ago by
NB
▴ 960
0
votes
0
replies
2.9k
views
Comment:
C: Downsample BAM for targeted NGS panels
5.6 years ago by
NB
▴ 960
0
votes
1
reply
2.9k
views
Comment:
C: Downsample BAM for targeted NGS panels
5.6 years ago by
NB
▴ 960
0
votes
1
reply
4.7k
views
Comment:
C: how to convert a list of genes to BED file?
5.7 years ago by
NB
▴ 960
0
votes
1
reply
5.2k
views
Comment:
C: How to extract SNPs from vcf file based on Population
5.7 years ago by
NB
▴ 960
0
votes
1
reply
2.1k
views
Comment:
C: File format for HGMD pro file flat
5.7 years ago by
NB
▴ 960
0
votes
1
reply
2.1k
views
Comment:
C: File format for HGMD pro file flat
5.7 years ago by
NB
▴ 960
0
votes
1
reply
2.1k
views
Comment:
C: File format for HGMD pro file flat
5.7 years ago by
NB
▴ 960
0
votes
7
replies
2.1k
views
File format for HGMD pro file flat
variant-analysis
HGMD
annovar
updated 18 months ago by
Ram
44k • written 5.7 years ago by
NB
▴ 960
3
votes
3
replies
1.7k
views
Extract info on OMIM Phenotype
OMIM
database
extract
updated 5.7 years ago by
GenoMax
146k • written 5.7 years ago by
NB
▴ 960
0
votes
0
replies
1.7k
views
Comment:
C: Extract info on OMIM Phenotype
5.7 years ago by
NB
▴ 960
1
vote
1
reply
2.5k
views
Comment:
C: GWAS data analysis strategy or pipeline
5.9 years ago by
NB
▴ 960
1
vote
0
replies
1.8k
views
Comment:
C: Alzheimer's disease and its classification
5.9 years ago by
NB
▴ 960
2
votes
1
reply
1.8k
views
Comment:
C: Alzheimer's disease and its classification
5.9 years ago by
NB
▴ 960
0
votes
0
replies
3.3k
views
Comment:
C: Difference in Haplotypecaller in GATKv4 Vs Gatk3.7
5.9 years ago by
NB
▴ 960
2
votes
5
replies
3.3k
views
Difference in Haplotypecaller in GATKv4 Vs Gatk3.7
gatk
haplotypecaller
updated 5.9 years ago by
lffu_0032
▴ 90 • written 6.0 years ago by
NB
▴ 960
0
votes
1
reply
3.3k
views
Comment:
C: Difference in Haplotypecaller in GATKv4 Vs Gatk3.7
5.9 years ago by
NB
▴ 960
1
vote
1
reply
2.2k
views
Comment:
C: CNV and pseudogenes
6.1 years ago by
NB
▴ 960
0
votes
1
reply
2.2k
views
Comment:
C: CNV and pseudogenes
6.1 years ago by
NB
▴ 960
0
votes
1
reply
2.2k
views
Comment:
C: CNV and pseudogenes
6.1 years ago by
NB
▴ 960
0
votes
0
replies
2.0k
views
Comment:
C: Tools to detect CNV for NGS-mtDNA
6.1 years ago by
NB
▴ 960
0
votes
1
reply
2.0k
views
Comment:
C: Tools to detect CNV for NGS-mtDNA
6.1 years ago by
NB
▴ 960
0
votes
4
replies
2.0k
views
Tools to detect CNV for NGS-mtDNA
mtDNA
NGS
updated 16 months ago by
Ram
44k • written 6.1 years ago by
NB
▴ 960
0
votes
1
reply
3.0k
views
Comment:
C: Detection of deletion for mitochondrial NGS analysis at position 3107
6.1 years ago by
NB
▴ 960
0
votes
0
replies
2.8k
views
Comment:
C: Next-Seq sequences map poorly to ref genome
6.1 years ago by
NB
▴ 960
0
votes
1
reply
2.7k
views
Comment:
C: Down sampling BAM files for CNV detection
6.1 years ago by
NB
▴ 960
0
votes
1
reply
2.7k
views
Comment:
C: Down sampling BAM files for CNV detection
6.1 years ago by
NB
▴ 960
0
votes
1
reply
2.8k
views
Comment:
C: Next-Seq sequences map poorly to ref genome
6.1 years ago by
NB
▴ 960
8
votes
7
replies
2.7k
views
Down sampling BAM files for CNV detection
dowsampling
BAM
CNV
NGS
updated 6.1 years ago by
WouterDeCoster
47k • written 6.1 years ago by
NB
▴ 960
0
votes
1
reply
2.8k
views
Comment:
C: Next-Seq sequences map poorly to ref genome
6.1 years ago by
NB
▴ 960
210 results • Page
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