Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
32
votes
10
replies
17k
views
8 follow
How to efficiently remove a list of reads from BAM file?
RNA-Seq BAM samtools Sam
updated 2.3 years ago by 3.1k • written 8.9 years ago by ▴ 540
9
votes
4
replies
8.6k
views
Genetic Map file format: how to understand the combined_rate column and the genetic_map column ?
genetic map centimorgan
updated 4.1 years ago by • 0 • written 8.0 years ago by ▴ 540
0
votes
0
replies
1.5k
views
Comment: C: Plink with hwe option does not work
4.5 years ago by Tao ▴ 540
0
votes
1
reply
1.5k
views
Answer: A: Plink with hwe option does not work
4.5 years ago by Tao ▴ 540
0
votes
1
reply
2.6k
views
Answer: A: color gradient for heatmap2
4.5 years ago by Tao ▴ 540
0
votes
0
replies
2.5k
views
Comment: C: How to quickly tell the reference allele given chr, pos, A1 and A2 allele?
4.5 years ago by Tao ▴ 540
0
votes
0
replies
2.5k
views
Comment: C: How to quickly tell the reference allele given chr, pos, A1 and A2 allele?
4.5 years ago by Tao ▴ 540
0
votes
4
replies
2.5k
views
How to quickly tell the reference allele given chr, pos, A1 and A2 allele?
snp reference allele ref allele
4.5 years ago by Tao ▴ 540
4
votes
0
replies
17k
views
Comment: C: How to efficiently remove a list of reads from BAM file?
updated 4.9 years ago by 44k • written 8.9 years ago by ▴ 540
0
votes
0
replies
17k
views
Comment: C: How to efficiently remove a list of reads from BAM file?
updated 4.9 years ago by 44k • written 8.9 years ago by ▴ 540
0
votes
0
replies
1.5k
views
Comment: C: Inspect the LD relation between a single pair of SNPs in detail using Plink --ld
5.0 years ago by Tao ▴ 540
0
votes
1
reply
1.5k
views
Comment: C: Inspect the LD relation between a single pair of SNPs in detail using Plink --ld
5.0 years ago by Tao ▴ 540
2
votes
4
replies
1.5k
views
Inspect the LD relation between a single pair of SNPs in detail using Plink --ld
plink --ld LD
updated 5.0 years ago by 11k • written 5.0 years ago by ▴ 540
0
votes
0
replies
3.7k
views
Comment: C: Recoding bim to vcf file with forcing allele-A1
5.4 years ago by Tao ▴ 540
0
votes
0
replies
1.2k
views
How to do Meta-analysis of statistics from T-tests and Wilcoxon rank sum tests?
meta analysis t test wilcoxon rank sum
5.5 years ago by Tao ▴ 540
2
votes
1
reply
2.6k
views
Answer: A: "hrc-1000g-check-bim.py" Unable to open specified bim file
5.5 years ago by Tao ▴ 540
0
votes
0
replies
1.5k
views
How to define the LD interval where a SNP locates?
LD genetics plink
6.0 years ago by Tao ▴ 540
8
votes
3
replies
2.5k
views
How to get gene full description with Ensembl IDs?
gene annotation Ensembl
updated 6.2 years ago by 12k • written 7.8 years ago by ▴ 540
0
votes
0
replies
1.8k
views
Answer: A: How to match alleles for a pair of SNPs using PLINK?
6.5 years ago by Tao ▴ 540
0
votes
1
reply
1.8k
views
How to match alleles for a pair of SNPs using PLINK?
LD Allele matching Plink
6.5 years ago by Tao ▴ 540
1
vote
1
reply
14k
views
Comment: C: Calculating TPM Values
6.6 years ago by Tao ▴ 540
5
votes
1
reply
14k
views
Answer: A: Calculating TPM Values
6.6 years ago by Tao ▴ 540
1
vote
0
replies
66k
views
Comment: Comment: RNA-seq: Explain STAR quantMode geneCounts values
6.6 years ago by Tao ▴ 540
1
vote
0
replies
12k
views
Comment: C: WGCNA signed vs unsigned network
7.0 years ago by Tao ▴ 540
6
votes
1
reply
12k
views
Answer: A: WGCNA signed vs unsigned network
7.0 years ago by Tao ▴ 540
0
votes
0
replies
18k
views
Comment: C: Filtering Imputation output: how to filter on a VCF INFO field
7.0 years ago by Tao ▴ 540
4
votes
0
replies
18k
views
Answer: A: What exactly is sequencing depth in RNAseq?
7.0 years ago by Tao ▴ 540
0
votes
1
reply
4.2k
views
Comment: C: Does it make sense to perform Genotype Imputation using variants called from WES
7.0 years ago by Tao ▴ 540
0
votes
1
reply
4.2k
views
Comment: C: Does it make sense to perform Genotype Imputation using variants called from WES
7.1 years ago by Tao ▴ 540
0
votes
0
replies
3.7k
views
Comment: C: Imputation on two genotyping datasets: should I do imputation separately? or mer
7.1 years ago by Tao ▴ 540
0
votes
1
reply
4.2k
views
Comment: C: Does it make sense to perform Genotype Imputation using variants called from WES
7.1 years ago by Tao ▴ 540
4
votes
7
replies
4.2k
views
Does it make sense to perform Genotype Imputation using variants called from WES?
genotype imputation Whole Exon Sequencing variants
7.1 years ago by Tao ▴ 540
1
vote
5
replies
4.8k
views
In GWAS Studies, how to understand "97 SNPs explain 2.7% of BMI"?
GWAS
updated 7.5 years ago by 8.7k • written 7.5 years ago by ▴ 540
0
votes
1
reply
4.8k
views
Comment: A: In GWAS Studies, how to understand "97 SNPs explain 2.7% of BMI"?
7.5 years ago by Tao ▴ 540
1
vote
1
reply
14k
views
Comment: C: How to remove a list of reads from fastq file?
7.5 years ago by Tao ▴ 540
1
vote
0
replies
4.0k
views
Answer: A: How to access VCF files for Genotype Tissue Expression (GTEx) data
7.8 years ago by Tao ▴ 540
0
votes
0
replies
18k
views
Answer: A: Filtering Imputation output: how to filter on a VCF INFO field
8.0 years ago by Tao ▴ 540
0
votes
0
replies
18k
views
Comment: C: Filtering Imputation output: how to filter on a VCF INFO field
8.0 years ago by Tao ▴ 540
1
vote
1
reply
2.1k
views
Answer: A: paste columns into one line in command line
8.0 years ago by Tao ▴ 540
1
vote
1
reply
3.7k
views
Imputation on two genotyping datasets: should I do imputation separately? or merge the two datasets first?
imputation genotyping eQTL SNPs
8.0 years ago by Tao ▴ 540
1
vote
0
replies
1.7k
views
Can I do eqtl mapping combining RNA-seq and Microarray data?
eqtl RNA-Seq microarray
8.3 years ago by Tao ▴ 540
0
votes
0
replies
5.5k
views
Answer: A: Paired-end RNA Seq data: How to deal with unpaired data after trimmomatic
8.3 years ago by Tao ▴ 540
0
votes
0
replies
14k
views
Comment: C: How to remove a list of reads from fastq file?
8.4 years ago by Tao ▴ 540
10
votes
9
replies
14k
views
6 follow
How to remove a list of reads from fastq file?
fastq shell bash script
updated 2.0 years ago by • 0 • written 8.4 years ago by ▴ 540
0
votes
1
reply
14k
views
Answer: A: How to remove a list of reads from fastq file?
8.4 years ago by Tao ▴ 540
0
votes
0
replies
14k
views
Comment: C: How to remove a list of reads from fastq file?
8.4 years ago by Tao ▴ 540
0
votes
0
replies
4.1k
views
Comment: C: Should I use reads with good quality but failed-vendor flag?
8.4 years ago by Tao ▴ 540
0
votes
1
reply
4.1k
views
Comment: C: Should I use reads with good quality but failed-vendor flag?
8.4 years ago by Tao ▴ 540
4
votes
7
replies
4.1k
views
Should I use reads with good quality but failed-vendor flag?
sam vendor failed sam flag chastity score
updated 8.4 years ago by ★ 1.2k • written 8.4 years ago by ▴ 540
0
votes
0
replies
4.1k
views
Comment: C: Should I use reads with good quality but failed-vendor flag?
8.4 years ago by Tao ▴ 540
77 results • Page 1 of 2
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6