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Comment: How to compare data in two files and print matching data of file1 and file2
3.0 years ago by
Kumar
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Comment: How to compare data in two files and print matching data of file1 and file2
3.0 years ago by
Kumar
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Comment: How to compare data in two files and print matching data of file1 and file2
3.0 years ago by
Kumar
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Comment: How to compare data in two files and print matching data of file1 and file2
3.0 years ago by
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Comment: How to capture the position of SNPs from the gene's locations
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Comment: LD-decay in a r2 vs distance(cm) plot
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Kumar
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Comment: How to capture the position of SNPs from the gene's locations
3.0 years ago by
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Comment: How the calculated the decay line by nonlinear regression to the LD plot?
3.0 years ago by
Kumar
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Comment: How to put the non-linear regression tendency line to the LD plot?
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Comment: Plotting Linkage Disequilibrium Decay Across The Genome
3.1 years ago by
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Comment: GWAS in Plink - phenotype file format
3.2 years ago by
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Comment: Mixed Linear Model and GWAS study
3.2 years ago by
Kumar
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C: Mixed Linear Model and GWAS study
3.2 years ago by
Kumar
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C: Mixed Linear Model and GWAS study
3.2 years ago by
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C: Workflow for structural variants from long read sequencing data
3.2 years ago by
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C: Mixed Linear Model and GWAS study
3.2 years ago by
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▴ 170
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2.3k
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Comment:
C: Mixed Linear Model and GWAS study
3.2 years ago by
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▴ 170
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2.3k
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Comment:
C: Mixed Linear Model and GWAS study
3.2 years ago by
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▴ 170
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2.3k
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Comment:
C: Mixed Linear Model and GWAS study
3.2 years ago by
Kumar
▴ 170
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2.3k
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Comment:
C: Mixed Linear Model and GWAS study
3.2 years ago by
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▴ 170
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2.3k
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C: Mixed Linear Model and GWAS study
3.2 years ago by
Kumar
▴ 170
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2.4k
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C: ERROR::: vcf to PLINK
3.2 years ago by
Kumar
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C: ERROR::: vcf to PLINK
3.2 years ago by
Kumar
▴ 170
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C: ERROR::: vcf to PLINK
3.2 years ago by
Kumar
▴ 170
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C: ERROR::: vcf to PLINK
3.2 years ago by
Kumar
▴ 170
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Comment:
C: ERROR::: vcf to PLINK
3.2 years ago by
Kumar
▴ 170
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1.5k
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Comment:
C: How to analyze Exome Seq data for GWAS
3.3 years ago by
Kumar
▴ 170
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1.0k
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Comment:
C: How to process metatranscriptomics data
updated 3.3 years ago by
seidel
11k • written 3.3 years ago by
Kumar
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1.6k
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C: Quantifying abundances of transcripts using kallisto
3.5 years ago by
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▴ 170
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Comment:
C: Quantifying abundances of transcripts using kallisto
3.5 years ago by
Kumar
▴ 170
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1.6k
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Comment:
C: Quantifying abundances of transcripts using kallisto
3.5 years ago by
Kumar
▴ 170
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1.2k
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Comment:
C: How to run DESeq2 for multiple factors
3.5 years ago by
Kumar
▴ 170
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1.3k
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Comment:
C: How to do unsupervised clustering of RNA-Seq data
3.5 years ago by
Kumar
▴ 170
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1.2k
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C: How to run DESeq2 for multiple factors
3.6 years ago by
Kumar
▴ 170
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1.2k
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Comment:
C: How to run DESeq2 for multiple factors
3.6 years ago by
Kumar
▴ 170
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1.2k
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Comment:
C: How to run DESeq2 for multiple factors
3.6 years ago by
Kumar
▴ 170
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0
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4.4k
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Comment:
C: How to analyze Illumina RNASeq data
3.6 years ago by
Kumar
▴ 170
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1
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1.2k
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Comment:
C: How to run DESeq2 for multiple factors
3.6 years ago by
Kumar
▴ 170
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1
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4.4k
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Comment:
C: How to analyze Illumina RNASeq data
3.6 years ago by
Kumar
▴ 170
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1
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2.2k
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Comment:
C: how to process vcf files for GWAS analysis
3.6 years ago by
Kumar
▴ 170
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0
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1.5k
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Comment:
C: How to analyze Exome Seq data for GWAS
3.6 years ago by
Kumar
▴ 170
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1
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1.5k
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Comment:
C: How to analyze Exome Seq data for GWAS
3.6 years ago by
Kumar
▴ 170
0
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1
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1.5k
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Comment:
C: How to analyze Exome Seq data for GWAS
3.6 years ago by
Kumar
▴ 170
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1
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1.5k
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Comment:
C: How to analyze Exome Seq data for GWAS
3.6 years ago by
Kumar
▴ 170
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1
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1.5k
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Comment:
C: How to analyze Exome Seq data for GWAS
3.6 years ago by
Kumar
▴ 170
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1
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1.5k
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Comment:
C: How to analyze Exome Seq data for GWAS
3.6 years ago by
Kumar
▴ 170
0
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1
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1.4k
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Comment:
C: DESeq2 analysis with high number of samples
3.7 years ago by
Kumar
▴ 170
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2.4k
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Comment:
C: How to do DESeq2 for Kallisto
3.7 years ago by
Kumar
▴ 170
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0
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4.5k
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Comment:
C: How to run STAR with multiple files
3.7 years ago by
Kumar
▴ 170
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1
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2.4k
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Comment:
C: How to do DESeq2 for Kallisto
3.7 years ago by
Kumar
▴ 170
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