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Answer: A: Infinium Global Screening Array-Why there are few rsids/chromosome positons with
5.6 years ago by ShirleyDai ▴ 50
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2
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4.0k
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How to prepare WEGO input files
WEGO Pathway analysis
updated 6.0 years ago by 5.9k • written 8.5 years ago by ▴ 50
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4.8k
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Comment: C: beta coefficient for METAL input
7.3 years ago by ShirleyDai ▴ 50
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24k
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Answer: Answer: Quick Way To Combine Two Datasets Using Only Common Markers
updated 2.2 years ago by 44k • written 7.4 years ago by ▴ 50
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3.4k
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Comment: A: imputation only choose one population as reference panel
7.6 years ago by ShirleyDai ▴ 50
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3.5k
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Answer: A: Metal - the commnad you issued could not be processed
7.6 years ago by ShirleyDai ▴ 50
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8.6k
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Answer: Answer: Get Rs Number Based On Position (6 million SNPs)
updated 2.2 years ago by 44k • written 7.6 years ago by ▴ 50
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5
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2.9k
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how to do further analysis after variant calling and annotation?
sequencing next-gen
updated 7.7 years ago by 20 • written 8.5 years ago by ▴ 50
9
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3
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5.4k
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errors in running smartpca
plink smartpca eigensoft GWAS
updated 7.7 years ago by 4.5k • written 8.2 years ago by ▴ 50
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8.8k
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Comment: C: Any better ways to filter GATK Mutect2 output?
7.8 years ago by ShirleyDai ▴ 50
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8.8k
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Comment: C: Any better ways to filter GATK Mutect2 output?
7.8 years ago by ShirleyDai ▴ 50
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5
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8.8k
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Any better ways to filter GATK Mutect2 output?
GATK Mutect2 VCF
updated 7.8 years ago by 13k • written 8.3 years ago by ▴ 50
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1
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2.4k
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Comment: C: Can I use exome sequencing data from cancer patient's blood to call germline var
7.9 years ago by ShirleyDai ▴ 50
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1
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2.4k
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Comment: C: Can I use exome sequencing data from cancer patient's blood to call germline var
7.9 years ago by ShirleyDai ▴ 50
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8
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2.4k
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Can I use exome sequencing data from cancer patient's blood to call germline variants?
GTAK sequencing
updated 7.9 years ago by ★ 3.2k • written 7.9 years ago by ▴ 50
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7.6k
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Comment: C: Genome-wide cox regression in R
7.9 years ago by ShirleyDai ▴ 50
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1
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17k
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Comment: C: Output from featureCounts() as input to DESeq2
8.0 years ago by ShirleyDai ▴ 50
1
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17k
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Comment: C: Output from featureCounts() as input to DESeq2
8.0 years ago by ShirleyDai ▴ 50
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2
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44k
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Comment: A: How To Analyze Imputed Gwas Data
8.0 years ago by ShirleyDai ▴ 50
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0
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5.4k
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Comment: C: errors in running smartpca
8.1 years ago by ShirleyDai ▴ 50
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4.0k
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Answer: A: Zero Trace error running Eigenstrat 5
8.2 years ago by ShirleyDai ▴ 50
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2.1k
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How to interpret CNV result and do visualization
CNV exomeCNV visualization
8.3 years ago by ShirleyDai ▴ 50
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1.4k
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Comment: C: Is there an integrated way to analyse mutation data and protein expression data
8.4 years ago by ShirleyDai ▴ 50
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1.4k
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Is there an integrated way to analyse mutation data and protein expression data
next-gen mutation immunohistochemistry
8.4 years ago by ShirleyDai ▴ 50
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1
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4.2k
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Answer: A: Haploview CG limit error?
8.4 years ago by ShirleyDai ▴ 50
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0
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101k
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Comment: C: Survival analysis of TCGA patients integrating gene expression (RNASeq) data
8.4 years ago by ShirleyDai ▴ 50
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2.2k
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Comment: C: Why some markers can be genotyped on chromosome y in female samples
8.4 years ago by ShirleyDai ▴ 50
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2
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2.2k
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Why some markers can be genotyped on chromosome y in female samples
plink gwas
8.4 years ago by ShirleyDai ▴ 50
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0
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101k
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Comment: C: Survival analysis of TCGA patients integrating gene expression (RNASeq) data
8.4 years ago by ShirleyDai ▴ 50
0
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1
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101k
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Comment: A: Survival analysis of TCGA patients integrating gene expression (RNASeq) data
8.4 years ago by ShirleyDai ▴ 50
0
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1
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101k
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Comment: A: Survival analysis of TCGA patients integrating gene expression (RNASeq) data
8.5 years ago by ShirleyDai ▴ 50
0
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3.3k
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How to run MutSigCV example correctly
musigcv
8.5 years ago by ShirleyDai ▴ 50
0
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0
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4.3k
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Comment: C: MutSig coverage table
8.5 years ago by ShirleyDai ▴ 50
2
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5
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5.1k
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How to extract both start and end position in vcf files
next-gen vcf
updated 8.5 years ago by ★ 2.1k • written 8.5 years ago by ▴ 50
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5.1k
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Comment: C: How to extract both start and end position in vcf files
8.5 years ago by ShirleyDai ▴ 50
0
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1
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5.1k
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Comment: C: How to extract both start and end position in vcf files
8.5 years ago by ShirleyDai ▴ 50
0
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1
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2.9k
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Comment: C: how to do further analysis after variant calling and annotation?
8.5 years ago by ShirleyDai ▴ 50
0
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1
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2.9k
views
Comment: C: how to do further analysis after variant calling and annotation?
8.5 years ago by ShirleyDai ▴ 50
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