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questions
0
votes
0
replies
381
views
the error as "ld: library not found for -lgfortran" in installing "clusterExperiment" package
cell
single
clusterExperiment
analysis
2.1 years ago by
xinhui.wang
▴ 550
0
votes
2
replies
659
views
how to convert from CpG island methylation array ID to target ID?
symbel
CpG
id
methylation
target
gene
IDs
island
array
2.2 years ago by
xinhui.wang
▴ 550
0
votes
0
replies
406
views
end to end workflow to import the download GEO data into tranSMART
tranSMART
GEO
2.6 years ago by
xinhui.wang
▴ 550
0
votes
1
reply
607
views
R script end to end meta analysis geo download data
microarray.
workflow
updated 2.6 years ago by
bigomics.team
▴ 90 • written 2.6 years ago by
xinhui.wang
▴ 550
0
votes
2
replies
552
views
how to extract each two columns from a matrix with Talend?
talned
2.8 years ago by
xinhui.wang
▴ 550
0
votes
1
reply
1.8k
views
Quality check for illumina GSA data
SNPs
Illumina
updated 3.5 years ago by
brinderbuttar
• 0 • written 6.9 years ago by
xinhui.wang
▴ 550
0
votes
2
replies
779
views
how to assembly the RNASeq data
RNA-Seq
Assembly
alignment
3.7 years ago by
xinhui.wang
▴ 550
0
votes
0
replies
426
views
LncRNA annotation tools( get ensembl_transcript_id from the position )
rna-seq
3.7 years ago by
xinhui.wang
▴ 550
0
votes
5
replies
784
views
gene ID translation
RNA-Seq
3.7 years ago by
xinhui.wang
▴ 550
0
votes
2
replies
995
views
ceRNA network identification
RNA-Seq
miRNA
mRNA
updated 3.8 years ago by
Biostar
20 • written 3.8 years ago by
xinhui.wang
▴ 550
63
votes
17
replies
37k
views
7 follow
how to remove multiallelic from VCF
SNP
updated 15 months ago by
Ram
43k • written 9.0 years ago by
xinhui.wang
▴ 550
0
votes
11
replies
1.7k
views
how to adjust a phenotype according to age
R
updated 5.1 years ago by
Ram
43k • written 5.1 years ago by
xinhui.wang
▴ 550
44
votes
7
replies
52k
views
How to extract sample id using bcftools or vcftools
SNP
vcf
bcftools
vcftools
updated 2.8 years ago by
Ă–mer An
▴ 260 • written 9.0 years ago by
xinhui.wang
▴ 550
3
votes
2
replies
3.2k
views
bsctools merge on duplicate samples
SNP
updated 18 months ago by
Ram
43k • written 8.8 years ago by
xinhui.wang
▴ 550
1
vote
1
reply
1.9k
views
How to generate genetics risk score with linkage disequilibrium?
SNPs
genetics risk score
linkage disequilibrium
updated 6.9 years ago by
Denise CS
★ 5.2k • written 6.9 years ago by
xinhui.wang
▴ 550
0
votes
0
replies
1.4k
views
genetic risk score generation with LD
SNP
gene
R
7.1 years ago by
xinhui.wang
▴ 550
0
votes
0
replies
2.8k
views
genetics risk score calculation
gene
7.4 years ago by
xinhui.wang
▴ 550
0
votes
3
replies
1.5k
views
risk value with genetic data
SNP
7.4 years ago by
xinhui.wang
▴ 550
1
vote
4
replies
3.1k
views
BWA and GATK pipeline
alignment
next-gen
Assembly
7.4 years ago by
xinhui.wang
▴ 550
0
votes
4
replies
3.6k
views
how to convert 012 data to ACTG data with plink?
SNP
updated 7.7 years ago by
akang
▴ 110 • written 8.9 years ago by
xinhui.wang
▴ 550
0
votes
1
reply
2.5k
views
Haplotype Association Tests
SNP
8.8 years ago by
xinhui.wang
▴ 550
0
votes
0
replies
1.7k
views
vcf to bed file with reference allele as 0
SNP
vcftools
updated 23 months ago by
Ram
43k • written 9.1 years ago by
xinhui.wang
▴ 550
1
vote
0
replies
2.4k
views
how to calculate the accuracy of imputation?
SNP
9.1 years ago by
xinhui.wang
▴ 550
4
votes
5
replies
3.5k
views
How to extractreference allele from fasta file
SNP
updated 10 months ago by
Ram
43k • written 9.1 years ago by
xinhui.wang
▴ 550
0
votes
5
replies
2.5k
views
vcftools for a zip file
software-error
updated 2.0 years ago by
Ram
43k • written 9.2 years ago by
xinhui.wang
▴ 550
4
votes
10
replies
3.2k
views
Snp'S On Exome Sequencing?
exome
sequencing
snp
10.9 years ago by
xinhui.wang
▴ 550
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