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Answer: A: Infinium Global Screening Array-Why there are few rsids/chromosome positons with
5.0 years ago by ShirleyDai ▴ 50
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2
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3.8k
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How to prepare WEGO input files
WEGO Pathway analysis
updated 5.4 years ago by 5.8k • written 7.9 years ago by ▴ 50
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4.4k
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Comment: C: beta coefficient for METAL input
6.7 years ago by ShirleyDai ▴ 50
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23k
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Answer: Answer: Quick Way To Combine Two Datasets Using Only Common Markers
updated 19 months ago by 43k • written 6.8 years ago by ▴ 50
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3.2k
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Comment: A: imputation only choose one population as reference panel
7.0 years ago by ShirleyDai ▴ 50
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3.1k
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Answer: A: Metal - the commnad you issued could not be processed
7.0 years ago by ShirleyDai ▴ 50
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7.5k
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Answer: Answer: Get Rs Number Based On Position (6 million SNPs)
updated 19 months ago by 43k • written 7.0 years ago by ▴ 50
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5
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how to do further analysis after variant calling and annotation?
sequencing next-gen
updated 7.1 years ago by 20 • written 7.9 years ago by ▴ 50
9
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3
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5.1k
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errors in running smartpca
plink smartpca eigensoft GWAS
updated 7.2 years ago by 4.2k • written 7.6 years ago by ▴ 50
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8.4k
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Comment: C: Any better ways to filter GATK Mutect2 output?
7.2 years ago by ShirleyDai ▴ 50
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8.4k
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Comment: C: Any better ways to filter GATK Mutect2 output?
7.2 years ago by ShirleyDai ▴ 50
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5
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8.4k
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Any better ways to filter GATK Mutect2 output?
GATK Mutect2 VCF
updated 7.2 years ago by 13k • written 7.8 years ago by ▴ 50
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1
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2.2k
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Comment: C: Can I use exome sequencing data from cancer patient's blood to call germline var
7.3 years ago by ShirleyDai ▴ 50
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1
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2.2k
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Comment: C: Can I use exome sequencing data from cancer patient's blood to call germline var
7.3 years ago by ShirleyDai ▴ 50
3
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8
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2.2k
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Can I use exome sequencing data from cancer patient's blood to call germline variants?
GTAK sequencing
updated 7.3 years ago by ★ 3.2k • written 7.3 years ago by ▴ 50
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Comment: C: Genome-wide cox regression in R
7.3 years ago by ShirleyDai ▴ 50
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1
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16k
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Comment: C: Output from featureCounts() as input to DESeq2
7.4 years ago by ShirleyDai ▴ 50
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16k
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Comment: C: Output from featureCounts() as input to DESeq2
7.4 years ago by ShirleyDai ▴ 50
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2
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43k
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Comment: A: How To Analyze Imputed Gwas Data
7.4 years ago by ShirleyDai ▴ 50
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0
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5.1k
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Comment: C: errors in running smartpca
7.5 years ago by ShirleyDai ▴ 50
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3.7k
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Answer: A: Zero Trace error running Eigenstrat 5
7.6 years ago by ShirleyDai ▴ 50
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2.0k
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How to interpret CNV result and do visualization
CNV exomeCNV visualization
7.7 years ago by ShirleyDai ▴ 50
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1.3k
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Comment: C: Is there an integrated way to analyse mutation data and protein expression data
7.8 years ago by ShirleyDai ▴ 50
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1.3k
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Is there an integrated way to analyse mutation data and protein expression data
next-gen mutation immunohistochemistry
7.8 years ago by ShirleyDai ▴ 50
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1
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3.9k
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Answer: A: Haploview CG limit error?
7.9 years ago by ShirleyDai ▴ 50
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95k
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Comment: C: Survival analysis of TCGA patients integrating gene expression (RNASeq) data
7.9 years ago by ShirleyDai ▴ 50
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2.1k
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Comment: C: Why some markers can be genotyped on chromosome y in female samples
7.9 years ago by ShirleyDai ▴ 50
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2
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2.1k
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Why some markers can be genotyped on chromosome y in female samples
plink gwas
7.9 years ago by ShirleyDai ▴ 50
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0
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95k
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Comment: C: Survival analysis of TCGA patients integrating gene expression (RNASeq) data
7.9 years ago by ShirleyDai ▴ 50
0
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1
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95k
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Comment: A: Survival analysis of TCGA patients integrating gene expression (RNASeq) data
7.9 years ago by ShirleyDai ▴ 50
0
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1
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95k
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Comment: A: Survival analysis of TCGA patients integrating gene expression (RNASeq) data
7.9 years ago by ShirleyDai ▴ 50
0
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0
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3.2k
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How to run MutSigCV example correctly
musigcv
7.9 years ago by ShirleyDai ▴ 50
0
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4.0k
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Comment: C: MutSig coverage table
7.9 years ago by ShirleyDai ▴ 50
2
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5
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4.9k
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How to extract both start and end position in vcf files
next-gen vcf
updated 7.9 years ago by ★ 2.1k • written 7.9 years ago by ▴ 50
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4.9k
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Comment: C: How to extract both start and end position in vcf files
7.9 years ago by ShirleyDai ▴ 50
0
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1
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4.9k
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Comment: C: How to extract both start and end position in vcf files
7.9 years ago by ShirleyDai ▴ 50
0
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1
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2.5k
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Comment: C: how to do further analysis after variant calling and annotation?
7.9 years ago by ShirleyDai ▴ 50
0
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1
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2.5k
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Comment: C: how to do further analysis after variant calling and annotation?
7.9 years ago by ShirleyDai ▴ 50
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