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Comment: Comment: VCF record format error when trying to run Beagle 5.4
9 months ago by r.tor ▴ 50
0
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2
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656
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VCF record format error when trying to run Beagle 5.4
VCF beagle java
updated 9 months ago by 43k • written 9 months ago by ▴ 50
0
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1
reply
809
views
Comment: Comment: Error when trying to make MetaXcan run through Snakemake
22 months ago by r.tor ▴ 50
1
vote
3
replies
809
views
Error when trying to make MetaXcan run through Snakemake
MetaXcan Python PrediXcan Snakemake
updated 22 months ago by 22k • written 22 months ago by ▴ 50
2
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3
replies
1.1k
views
Counting the number of SNPs (VCF) for each genomic coordinates (BED)
vcf vcftools bed bedtools
updated 2.5 years ago by ▴ 100 • written 2.5 years ago by ▴ 50
0
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1.1k
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Comment: Comment: Counting the number of SNPs (VCF) for each genomic coordinates (BED)
2.5 years ago by r.tor ▴ 50
4
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7
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1.9k
views
Merge coordinates by gene ID
BEDOPS BASH BEDTOOLS BED
3.5 years ago by r.tor ▴ 50
0
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0
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1.9k
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Comment: C: Merge coordinates by gene ID
3.5 years ago by r.tor ▴ 50
0
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1
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1.9k
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Comment: C: Merge coordinates by gene ID
3.5 years ago by r.tor ▴ 50
0
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0
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1.9k
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Comment: C: Merge coordinates by gene ID
3.5 years ago by r.tor ▴ 50
1
vote
1
reply
801
views
Split up a matrix into chunks considering the values of a column in Bash
bash shell
3.9 years ago by r.tor ▴ 50
0
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0
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1.0k
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Where to get population diversity information of GTEx database?
GTEx pca rna-seq
5.0 years ago by r.tor ▴ 50
11
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5
replies
1.5k
views
How to generate a short sequence that does not align to the hg38?
R alignment
5.2 years ago by r.tor ▴ 50
0
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0
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4.7k
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Comment: C: Create snakefile based on R script
5.3 years ago by r.tor ▴ 50
0
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3
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4.7k
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Comment: C: Create snakefile based on R script
5.3 years ago by r.tor ▴ 50
6
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9
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4.7k
views
Create snakefile based on R script
R snakemake python snakefile
updated 5.3 years ago by 47k • written 5.3 years ago by ▴ 50
0
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1
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4.7k
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Comment: C: Create snakefile based on R script
5.3 years ago by r.tor ▴ 50
0
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1
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5.1k
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Comment: C: Extracting Flanking Regions across TSS using R scripts
5.4 years ago by r.tor ▴ 50
0
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1
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5.1k
views
Comment: C: Extracting Flanking Regions across TSS using R scripts
5.4 years ago by r.tor ▴ 50
7
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6
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5.1k
views
Extracting Flanking Regions across TSS using R scripts
TSS R Bioconductor Coding ensembl
updated 5.4 years ago by ★ 3.4k • written 5.4 years ago by ▴ 50
0
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1
reply
1.8k
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Comment: C: Sequence alignment algorithm for big size genes in MATLAB
6.9 years ago by r.tor ▴ 50
0
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1
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1.8k
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Comment: C: Sequence alignment algorithm for big size genes in MATLAB
6.9 years ago by r.tor ▴ 50
0
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0
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1.8k
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Comment: C: Sequence alignment algorithm for big size genes in MATLAB
6.9 years ago by r.tor ▴ 50
8
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8
replies
1.8k
views
Sequence alignment algorithm for big size genes in MATLAB
alignment Matlab next-gen
6.9 years ago by r.tor ▴ 50
0
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0
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1.7k
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Comment: C: How I can explain the difference in gene size in hg19 and NG genome coordinates?
7.1 years ago by r.tor ▴ 50
0
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1
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1.7k
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Comment: C: How I can explain the difference in gene size in hg19 and NG genome coordinates?
7.1 years ago by r.tor ▴ 50
0
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4
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1.7k
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How I can explain the difference in gene size in hg19 and NG genome coordinates?
coding NGS Assembly gene next-gen
7.1 years ago by r.tor ▴ 50
0
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1
reply
1.8k
views
What is the appropriate approach for CNV and loss of heterozygosity analysis?
array cancer heterozygosity CGH SNP
7.2 years ago by r.tor ▴ 50
0
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0
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2.2k
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Comment: C: What is the difference between using genome build hg18 and hg19 in Genome-wide S
7.2 years ago by r.tor ▴ 50
1
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4
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2.2k
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What is the difference between using genome build hg18 and hg19 in Genome-wide SNP arrays?
CNVs analysis genome next-gen genome coordinate
7.2 years ago by r.tor ▴ 50
0
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1
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2.2k
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Answer: A: What is the difference between using genome build hg18 and hg19 in Genome-wide S
7.2 years ago by r.tor ▴ 50
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