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0
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581
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the error as "ld: library not found for -lgfortran" in installing "clusterExperiment" package
cell single clusterExperiment analysis
3.6 years ago by xinhui.wang ▴ 570
0
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0
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1.1k
views
Comment: Comment: how to convert from CpG island methylation array ID to target ID?
3.8 years ago by xinhui.wang ▴ 570
0
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2
replies
1.1k
views
how to convert from CpG island methylation array ID to target ID?
symbel CpG id methylation target gene IDs island array
3.8 years ago by xinhui.wang ▴ 570
0
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0
replies
625
views
end to end workflow to import the download GEO data into tranSMART
tranSMART GEO
4.1 years ago by xinhui.wang ▴ 570
0
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1
reply
1.0k
views
R script end to end meta analysis geo download data
microarray. workflow
updated 4.1 years ago by ▴ 90 • written 4.1 years ago by ▴ 570
0
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0
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964
views
Comment: Comment: how to extract each two columns from a matrix with Talend?
4.4 years ago by xinhui.wang ▴ 570
0
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2
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964
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how to extract each two columns from a matrix with Talend?
talned
4.4 years ago by xinhui.wang ▴ 570
0
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1
reply
2.1k
views
Quality check for illumina GSA data
SNPs Illumina
updated 5.0 years ago by • 0 • written 8.4 years ago by ▴ 570
0
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0
replies
1.1k
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Comment: C: how to assembly the RNASeq data
5.2 years ago by xinhui.wang ▴ 570
0
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2
replies
1.1k
views
how to assembly the RNASeq data
RNA-Seq Assembly alignment
5.2 years ago by xinhui.wang ▴ 570
0
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0
replies
612
views
LncRNA annotation tools( get ensembl_transcript_id from the position )
rna-seq
5.2 years ago by xinhui.wang ▴ 570
0
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0
replies
1.3k
views
Comment: C: gene ID translation
5.2 years ago by xinhui.wang ▴ 570
0
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1
reply
1.3k
views
Comment: C: gene ID translation
5.2 years ago by xinhui.wang ▴ 570
0
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5
replies
1.3k
views
gene ID translation
RNA-Seq
5.2 years ago by xinhui.wang ▴ 570
0
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0
replies
1.5k
views
Comment: C: ceRNA network identification
5.2 years ago by xinhui.wang ▴ 570
0
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2
replies
1.5k
views
ceRNA network identification
RNA-Seq miRNA mRNA
updated 5.3 years ago by 20 • written 5.3 years ago by ▴ 570
65
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17
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45k
views
7 follow
how to remove multiallelic from VCF
SNP
updated 2.7 years ago by 45k • written 10.5 years ago by ▴ 570
0
votes
11
replies
2.7k
views
how to adjust a phenotype according to age
R
updated 6.6 years ago by 45k • written 6.6 years ago by ▴ 570
0
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1
reply
2.7k
views
Comment: C: how to adjust a phenotype according to age
6.6 years ago by xinhui.wang ▴ 570
0
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1
reply
2.7k
views
Comment: C: how to adjust a phenotype according to age
6.6 years ago by xinhui.wang ▴ 570
0
votes
1
reply
2.7k
views
Comment: C: how to adjust a phenotype according to age
6.6 years ago by xinhui.wang ▴ 570
0
votes
1
reply
2.7k
views
Comment: C: how to adjust a phenotype according to age
6.6 years ago by xinhui.wang ▴ 570
46
votes
7
replies
62k
views
How to extract sample id using bcftools or vcftools
SNP vcf bcftools vcftools
updated 4.3 years ago by ▴ 270 • written 10.5 years ago by ▴ 570
33
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1
reply
62k
views
Answer: A: how to extract sample id with bcftools or vcftools
updated 7.0 years ago by 12k • written 10.5 years ago by ▴ 570
3
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2
replies
3.6k
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bsctools merge on duplicate samples
SNP
updated 3.0 years ago by 45k • written 10.3 years ago by ▴ 570
1
vote
1
reply
2.3k
views
How to generate genetics risk score with linkage disequilibrium?
SNPs genetics risk score linkage disequilibrium
updated 8.4 years ago by ★ 5.2k • written 8.4 years ago by ▴ 570
0
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0
replies
1.6k
views
genetic risk score generation with LD
SNP gene R
8.6 years ago by xinhui.wang ▴ 570
0
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0
replies
3.2k
views
genetics risk score calculation
gene
8.9 years ago by xinhui.wang ▴ 570
0
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1
reply
2.0k
views
Comment: C: risk value with genetic data
8.9 years ago by xinhui.wang ▴ 570
0
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1
reply
3.6k
views
Comment: C: BWA and GATK pipeline
8.9 years ago by xinhui.wang ▴ 570
0
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3
replies
2.0k
views
risk value with genetic data
SNP
8.9 years ago by xinhui.wang ▴ 570
1
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4
replies
3.6k
views
BWA and GATK pipeline
alignment next-gen Assembly
8.9 years ago by xinhui.wang ▴ 570
0
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4
replies
4.3k
views
how to convert 012 data to ACTG data with plink?
SNP
updated 9.2 years ago by ▴ 120 • written 10.4 years ago by ▴ 570
0
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0
replies
3.6k
views
Comment: C: bsctools merge on duplicate samples
10.3 years ago by xinhui.wang ▴ 570
0
votes
1
reply
2.7k
views
Haplotype Association Tests
SNP
10.3 years ago by xinhui.wang ▴ 570
0
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1
reply
4.3k
views
Comment: C: how to convert 012 data to ACTG data with plink?
10.4 years ago by xinhui.wang ▴ 570
0
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0
replies
2.0k
views
vcf to bed file with reference allele as 0
SNP vcftools
updated 3.5 years ago by 45k • written 10.6 years ago by ▴ 570
0
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1
reply
45k
views
Comment: C: how to remove multiallelic from VCF
10.5 years ago by xinhui.wang ▴ 570
0
votes
1
reply
45k
views
Comment: Comment: how to remove multiallelic from VCF
updated 2.7 years ago by 45k • written 10.5 years ago by ▴ 570
0
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0
replies
45k
views
Comment: C: how to remove multiallelic from VCF
10.5 years ago by xinhui.wang ▴ 570
1
vote
0
replies
62k
views
Comment: C: how to extract sample id with bcftools or vcftools
10.5 years ago by xinhui.wang ▴ 570
1
vote
0
replies
2.7k
views
how to calculate the accuracy of imputation?
SNP
10.6 years ago by xinhui.wang ▴ 570
0
votes
1
reply
4.1k
views
Comment: Comment: How to extractreference allele from fasta file
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 570
0
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1
reply
4.1k
views
Comment: C: How to extractreference allele from fasta file
10.6 years ago by xinhui.wang ▴ 570
4
votes
5
replies
4.1k
views
How to extractreference allele from fasta file
SNP
updated 2.4 years ago by 45k • written 10.6 years ago by ▴ 570
0
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5
replies
3.0k
views
vcftools for a zip file
software-error
updated 3.5 years ago by 45k • written 10.7 years ago by ▴ 570
0
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0
replies
4.5k
views
Answer: A: Snp'S On Exome Sequencing?
12.4 years ago by xinhui.wang ▴ 570
4
votes
10
replies
4.5k
views
Snp'S On Exome Sequencing?
exome sequencing snp
12.4 years ago by xinhui.wang ▴ 570
0
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1
reply
4.5k
views
Comment: C: Snp'S On Exome Sequencing?
12.4 years ago by xinhui.wang ▴ 570
0
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0
replies
4.5k
views
Comment: C: Snp'S On Exome Sequencing?
12.4 years ago by xinhui.wang ▴ 570
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