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stevenlang123
stevenlang123
Reputation:
210
Joined:
12.1 years ago
Last seen:
10.6 years ago
Location:
United States
Latest posts by user
2 votes
0 replies
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Answer: A: geneid.txt and knownGene.txt files in UCSC database to retrieve exon position in
updated by Ram Ram • written by stevenlang123 stevenlang123
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0 replies
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Comment: C: geneid.txt and knownGene.txt files in UCSC database to retrieve exon position in
updated by Ram Ram • written by stevenlang123 stevenlang123
0 votes
1 reply
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Comment: C: Calculation of PFBs for CNV analysis from 1000 Genomes data
updated by Ram Ram • written by stevenlang123 stevenlang123
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Comment: C: Cnv Calling Methods For The Illumina Omni2.5 - Penncnv And Quantisnp Possible?
written by stevenlang123 stevenlang123
0 votes
2 replies
2.4K views
Restrict ANNOVAR annotation to a list of genes.
genome next-gen sequencing
written by stevenlang123 stevenlang123
0 votes
4 replies
2.6K views
What is the best brand of external drive for storing NGS data ?
ngs snp data-storage genome-sequencing
updated by Ram Ram • written by stevenlang123 stevenlang123
0 votes
1 reply
11K views
Negative P-Values
gene genome next-gen-sequencing
updated by Ram Ram • written by stevenlang123 stevenlang123
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0 replies
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Comment: C: Next-generation DNA sequencing: How to tell systematic errors from real SNVs?
written by stevenlang123 stevenlang123
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1 reply
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Answer: Answer: Next-generation DNA sequencing: How to tell systematic errors from real SNVs?
updated by Ram Ram • written by stevenlang123 stevenlang123
0 votes
0 replies
1.6K views
Impute missing GT based on AF ?
r snp next-gen-sequencing
updated by Ram Ram • written by stevenlang123 stevenlang123
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0 replies
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Comment: C: bgzip all VCFs in a directory
written by stevenlang123 stevenlang123
0 votes
1 reply
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Comment: C: bgzip all VCFs in a directory
updated by Ram Ram • written by stevenlang123 stevenlang123
4 votes
5 replies
13K views
bgzip all VCFs in a directory
sequencing seq
updated by Ram Ram • written by stevenlang123 stevenlang123
0 votes
1 reply
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Comment: C: Recommendations on PLINK for CNV analysis
written by stevenlang123 stevenlang123
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Comment: Comment: Extract variant positions from single sample VCFs prior to merging ?
updated by Ram Ram • written by stevenlang123 stevenlang123
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1 reply
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Comment: Comment: Extract variant positions from single sample VCFs prior to merging ?
updated by Ram Ram • written by stevenlang123 stevenlang123
0 votes
5 replies
3.3K views
Extract variant positions from single sample VCFs prior to merging ?
sequencing snp sequence
updated by Ram Ram • written by stevenlang123 stevenlang123
0 votes
0 replies
1.5K views
What percent of the exome are low complexity targets?
plink exome-sequencing
updated by Ram Ram • written by stevenlang123 stevenlang123
2 votes
1 reply
2.3K views
Differential Methylation Interpretation
methylation epigenetics snp next-gen-sequencing
updated by Ram Ram • written by stevenlang123 stevenlang123
0 votes
0 replies
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Comment: C: Input GSEA Pre-ranked list
written by stevenlang123 stevenlang123
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