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Comment: Comment: VCF record format error when trying to run Beagle 5.4
17 months ago by r.tor ▴ 50
0
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2
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1000
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VCF record format error when trying to run Beagle 5.4
VCF beagle java
updated 17 months ago by 44k • written 17 months ago by ▴ 50
0
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1
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982
views
Comment: Comment: Error when trying to make MetaXcan run through Snakemake
2.5 years ago by r.tor ▴ 50
1
vote
3
replies
982
views
Error when trying to make MetaXcan run through Snakemake
MetaXcan Python PrediXcan Snakemake
updated 2.5 years ago by 22k • written 2.5 years ago by ▴ 50
2
votes
3
replies
1.3k
views
Counting the number of SNPs (VCF) for each genomic coordinates (BED)
vcf vcftools bed bedtools
updated 3.1 years ago by ▴ 100 • written 3.1 years ago by ▴ 50
0
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1
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1.3k
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Comment: Comment: Counting the number of SNPs (VCF) for each genomic coordinates (BED)
3.1 years ago by r.tor ▴ 50
4
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7
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2.3k
views
Merge coordinates by gene ID
BEDOPS BASH BEDTOOLS BED
4.1 years ago by r.tor ▴ 50
0
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0
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2.3k
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Comment: C: Merge coordinates by gene ID
4.1 years ago by r.tor ▴ 50
0
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1
reply
2.3k
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Comment: C: Merge coordinates by gene ID
4.1 years ago by r.tor ▴ 50
0
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0
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2.3k
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Comment: C: Merge coordinates by gene ID
4.1 years ago by r.tor ▴ 50
1
vote
1
reply
915
views
Split up a matrix into chunks considering the values of a column in Bash
bash shell
4.5 years ago by r.tor ▴ 50
0
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0
replies
1.1k
views
Where to get population diversity information of GTEx database?
GTEx pca rna-seq
5.6 years ago by r.tor ▴ 50
11
votes
5
replies
1.8k
views
How to generate a short sequence that does not align to the hg38?
R alignment
5.9 years ago by r.tor ▴ 50
0
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0
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4.9k
views
Comment: C: Create snakefile based on R script
5.9 years ago by r.tor ▴ 50
0
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3
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4.9k
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Comment: C: Create snakefile based on R script
5.9 years ago by r.tor ▴ 50
6
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9
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4.9k
views
Create snakefile based on R script
R snakemake python snakefile
updated 5.9 years ago by 47k • written 5.9 years ago by ▴ 50
0
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1
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4.9k
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Comment: C: Create snakefile based on R script
5.9 years ago by r.tor ▴ 50
0
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1
reply
5.4k
views
Comment: C: Extracting Flanking Regions across TSS using R scripts
6.0 years ago by r.tor ▴ 50
0
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1
reply
5.4k
views
Comment: C: Extracting Flanking Regions across TSS using R scripts
6.0 years ago by r.tor ▴ 50
7
votes
6
replies
5.4k
views
Extracting Flanking Regions across TSS using R scripts
TSS R Bioconductor Coding ensembl
updated 6.0 years ago by ★ 3.4k • written 6.0 years ago by ▴ 50
0
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1
reply
2.1k
views
Comment: C: Sequence alignment algorithm for big size genes in MATLAB
7.5 years ago by r.tor ▴ 50
0
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1
reply
2.1k
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Comment: C: Sequence alignment algorithm for big size genes in MATLAB
7.5 years ago by r.tor ▴ 50
0
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0
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2.1k
views
Comment: C: Sequence alignment algorithm for big size genes in MATLAB
7.5 years ago by r.tor ▴ 50
8
votes
8
replies
2.1k
views
Sequence alignment algorithm for big size genes in MATLAB
alignment Matlab next-gen
7.5 years ago by r.tor ▴ 50
0
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0
replies
1.8k
views
Comment: C: How I can explain the difference in gene size in hg19 and NG genome coordinates?
7.7 years ago by r.tor ▴ 50
0
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1
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1.8k
views
Comment: C: How I can explain the difference in gene size in hg19 and NG genome coordinates?
7.7 years ago by r.tor ▴ 50
0
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4
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1.8k
views
How I can explain the difference in gene size in hg19 and NG genome coordinates?
coding NGS Assembly gene next-gen
7.7 years ago by r.tor ▴ 50
0
votes
1
reply
1.9k
views
What is the appropriate approach for CNV and loss of heterozygosity analysis?
array cancer heterozygosity CGH SNP
7.8 years ago by r.tor ▴ 50
0
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0
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2.4k
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Comment: C: What is the difference between using genome build hg18 and hg19 in Genome-wide S
7.8 years ago by r.tor ▴ 50
0
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1
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2.4k
views
Answer: A: What is the difference between using genome build hg18 and hg19 in Genome-wide S
7.8 years ago by r.tor ▴ 50
1
vote
4
replies
2.4k
views
What is the difference between using genome build hg18 and hg19 in Genome-wide SNP arrays?
CNVs analysis genome next-gen genome coordinate
7.8 years ago by r.tor ▴ 50
31 results • Page 1 of 1
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