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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
John Marshall
3.1k • written 8.9 years ago by
Tao
▴ 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
2649935201
• 0 • written 8.0 years ago by
Tao
▴ 540
0
votes
0
replies
1.5k
views
Comment:
C: Plink with hwe option does not work
4.6 years ago by
Tao
▴ 540
0
votes
1
reply
1.5k
views
Answer:
A: Plink with hwe option does not work
4.6 years ago by
Tao
▴ 540
0
votes
1
reply
2.6k
views
Answer:
A: color gradient for heatmap2
4.6 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?
4.6 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?
4.6 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
4.6 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
Ram
44k • written 8.9 years ago by
Tao
▴ 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
Ram
44k • written 8.9 years ago by
Tao
▴ 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
chrchang523
11k • written 5.0 years ago by
Tao
▴ 540
0
votes
0
replies
3.7k
views
Comment:
C: Recoding bim to vcf file with forcing allele-A1
5.5 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
5.6 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
5.6 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
zx8754
12k • written 7.8 years ago by
Tao
▴ 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
6.7 years ago by
Tao
▴ 540
5
votes
1
reply
14k
views
Answer:
A: Calculating TPM Values
6.7 years ago by
Tao
▴ 540
1
vote
0
replies
66k
views
Comment:
Comment: RNA-seq: Explain STAR quantMode geneCounts values
6.7 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?
7.1 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
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
Philipp Bayer
8.8k • written 7.5 years ago by
Tao
▴ 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
Viki
• 0 • written 8.4 years ago by
Tao
▴ 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
ablanchetcohen
★ 1.2k • written 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
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