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Comment: C: Annotate Variants with Pharmacogenomic Data
updated 4.9 years ago by 44k • written 10.4 years ago by ▴ 120
5
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5
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3.8k
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Coverage analysis of NGS data by Depth
NGS panels depth coverage
updated 7.2 years ago by ▴ 20 • written 7.4 years ago by ▴ 120
0
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1
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3.8k
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Comment: C: Coverage analysis of NGS data by Depth
7.4 years ago by nilakshafreezon ▴ 120
0
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1
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6.6k
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Comment: C: Filterout biallelic SNPs from multiple VCF files.
10.0 years ago by nilakshafreezon ▴ 120
6
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5
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6.6k
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Filterout biallelic SNPs from multiple VCF files.
HLA vcf bi allelic SNP
updated 2.8 years ago by 44k • written 10.0 years ago by ▴ 120
1
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0
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5.4k
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Comment: C: Efficient strategy for remote blasting of 3000 sequences
10.3 years ago by nilakshafreezon ▴ 120
0
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0
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4.2k
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Comment: C: HLA typing analysis with plink or any other method?
10.3 years ago by nilakshafreezon ▴ 120
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0
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4.2k
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Comment: Comment: HLA typing analysis with plink or any other method?
updated 2.9 years ago by 44k • written 10.3 years ago by ▴ 120
2
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4
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4.2k
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HLA typing analysis with plink or any other method?
HLA plink
updated 2.9 years ago by 44k • written 10.3 years ago by ▴ 120
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0
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2.7k
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Comment: C: pathway analysis tools
10.3 years ago by nilakshafreezon ▴ 120
0
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1
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4.0k
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Comment: C: multisample BED files to PED conversion
10.3 years ago by nilakshafreezon ▴ 120
0
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1
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4.0k
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Comment: C: multisample BED files to PED conversion
10.3 years ago by nilakshafreezon ▴ 120
1
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1
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2.7k
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Answer: A: pathway analysis tools
10.3 years ago by nilakshafreezon ▴ 120
0
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1
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4.0k
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Comment: Comment: multisample BED files to PED conversion
updated 3.0 years ago by 44k • written 10.4 years ago by ▴ 120
2
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7
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4.0k
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multisample BED files to PED conversion
plink ped gwas Bed VCF
updated 3.0 years ago by 44k • written 10.4 years ago by ▴ 120
2
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0
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3.3k
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GATK: High quality value error
genome sequencing SNP next-gen
updated 3.0 years ago by 44k • written 10.4 years ago by ▴ 120
2
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0
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4.8k
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Answer: Answer: ClinVar Mutation representations and Descriptions
updated 3.1 years ago by 44k • written 10.4 years ago by ▴ 120
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0
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2.9k
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Answer: Answer: How to differentiate between protective and damaging variants
updated 3.1 years ago by 44k • written 10.4 years ago by ▴ 120
0
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0
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3.1k
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Comment: Comment: Finding important predispositions using R
updated 3.1 years ago by 44k • written 10.4 years ago by ▴ 120
0
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1
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3.1k
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Comment: C: Finding important predispositions using R
10.4 years ago by nilakshafreezon ▴ 120
8
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8
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3.1k
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Finding important predispositions using R
R ClinVar
updated 20 months ago by 44k • written 10.4 years ago by ▴ 120
0
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0
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3.1k
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Comment: Comment: Finding important predispositions using R
updated 3.1 years ago by 44k • written 10.4 years ago by ▴ 120
0
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2
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2.7k
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Annotate Variants with Pharmacogenomic Data
pharmacogenomics ngs Exome sequencing
updated 10.4 years ago by ★ 1.9k • written 10.4 years ago by ▴ 120
0
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0
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1.9k
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Comment: C: Identifying transcripts from exome sequencing?!!
10.5 years ago by nilakshafreezon ▴ 120
3
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2
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1.9k
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Identifying transcripts from exome sequencing?!!
SNP sequencing genome gene
updated 10.5 years ago by 104k • written 10.5 years ago by ▴ 120
0
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0
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4.6k
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Comment: C: Using A Cluster Of Macs To Share Computational Power
10.6 years ago by nilakshafreezon ▴ 120
2
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2
replies
4.6k
views
Using A Cluster Of Macs To Share Computational Power
updated 10.6 years ago by 35k • written 10.6 years ago by ▴ 120
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