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Comment: C: Sizes of Nanopore files and how to store?
4.0 years ago by Floris Brenk ★ 1.0k
3
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40k
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Comment: C: 1000 Genomes Ld Calculation
updated 4.6 years ago by 43k • written 10.3 years ago by ★ 1.0k
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0
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2.4k
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Comment: C: Allele Frequency correlation in R
updated 5.6 years ago by 43k • written 8.2 years ago by ★ 1.0k
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1
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2.5k
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Comment: C: Remove rows based on duplicates in one column
updated 5.6 years ago by 43k • written 8.2 years ago by ★ 1.0k
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0
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1.9k
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Comment: C: XHMM GATK exome sequencing deletions genome wide or selected genes ?
updated 5.6 years ago by 43k • written 8.2 years ago by ★ 1.0k
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5.3k
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Comment: C: ATACseq and HiC sequencing
6.5 years ago by Floris Brenk ★ 1.0k
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1
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5.3k
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Comment: C: ATACseq and HiC sequencing
6.5 years ago by Floris Brenk ★ 1.0k
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3.8k
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Comment: C: How to make a nice mutation overview figure like this?
6.7 years ago by Floris Brenk ★ 1.0k
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0
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3.8k
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Comment: C: How to make a nice mutation overview figure like this?
6.7 years ago by Floris Brenk ★ 1.0k
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0
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1.7k
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Comment: C: extract SNPs (rs.....) along with subject ID and pedigree ID in PLINK
6.8 years ago by Floris Brenk ★ 1.0k
1
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0
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8.0k
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Comment: C: Imputation of chromosome X using the Michigan imputation server
6.8 years ago by Floris Brenk ★ 1.0k
0
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1
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2.5k
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Comment: C: Chromosome Y imputation, any good reference panels?
7.0 years ago by Floris Brenk ★ 1.0k
0
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0
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8.0k
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Comment: C: Imputation of chromosome X using the Michigan imputation server
7.0 years ago by Floris Brenk ★ 1.0k
0
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1
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6.0k
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Comment: C: Cannot remove subjects from Plink files
7.0 years ago by Floris Brenk ★ 1.0k
0
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1
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8.0k
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Comment: C: Imputation of chromosome X using the Michigan imputation server
7.0 years ago by Floris Brenk ★ 1.0k
0
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1
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9.4k
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Comment: C: How to annotate TTS or TES
7.2 years ago by Floris Brenk ★ 1.0k
0
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0
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2.1k
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Comment: C: RNA seq library preparation, PCR cycles
7.2 years ago by Floris Brenk ★ 1.0k
0
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1
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2.7k
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Comment: C: vcftools merge files problem
7.4 years ago by Floris Brenk ★ 1.0k
0
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1
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2.7k
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Comment: C: vcftools merge files problem
7.4 years ago by Floris Brenk ★ 1.0k
0
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0
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1.5k
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Comment: C: risk value with genetic data
7.4 years ago by Floris Brenk ★ 1.0k
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0
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1.5k
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Comment: C: Ped file contains: 0, -, multibase SNPs, and reverse order genotypes
7.4 years ago by Floris Brenk ★ 1.0k
1
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1
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2.7k
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Comment: C: How I can convert genotype data in a variety of pedigree formats R
7.4 years ago by Floris Brenk ★ 1.0k
0
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1
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2.4k
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Comment: C: Dealing with abnormally high coverage regions
7.5 years ago by Floris Brenk ★ 1.0k
0
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1
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1.6k
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Comment: C: Detect chromosome abnormalities in WGS
7.5 years ago by Floris Brenk ★ 1.0k
0
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1
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1.6k
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Comment: C: Detect chromosome abnormalities in WGS
7.5 years ago by Floris Brenk ★ 1.0k
0
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1
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1.6k
views
Comment: C: Detect chromosome abnormalities in WGS
7.5 years ago by Floris Brenk ★ 1.0k
0
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1
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2.6k
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Comment: C: Identification of haplotype blocks
7.5 years ago by Floris Brenk ★ 1.0k
1
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1
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9.7k
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Comment: C: How do people know to use at least 30X coverage in WGS?
7.5 years ago by Floris Brenk ★ 1.0k
0
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0
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17k
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Comment: C: Filtering Imputation output: how to filter on a VCF INFO field
7.5 years ago by Floris Brenk ★ 1.0k
0
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0
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2.6k
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Comment: C: Using PLINK to check SNP variation for a gene
7.6 years ago by Floris Brenk ★ 1.0k
0
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0
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2.2k
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Comment: C: SNP running using imputed genotype
7.6 years ago by Floris Brenk ★ 1.0k
0
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1
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2.2k
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Comment: C: SNP running using imputed genotype
7.6 years ago by Floris Brenk ★ 1.0k
1
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0
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2.1k
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Comment: C: genotype imputation - alleles
7.7 years ago by Floris Brenk ★ 1.0k
0
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0
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8.6k
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Comment: C: convert imputed genotypes in VCF file to plink format
7.7 years ago by Floris Brenk ★ 1.0k
1
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0
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2.3k
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Comment: C: Convert SNP from A_B format into plink using R package
7.7 years ago by Floris Brenk ★ 1.0k
1
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0
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2.2k
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Comment: C: Creating intergenic bam file
7.7 years ago by Floris Brenk ★ 1.0k
1
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0
replies
5.2k
views
Comment: C: Allele count for SNPs
7.7 years ago by Floris Brenk ★ 1.0k
0
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0
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2.8k
views
Comment: C: GTEx genotype data
7.8 years ago by Floris Brenk ★ 1.0k
0
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1
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4.6k
views
Comment: C: R: read.plink Error
7.8 years ago by Floris Brenk ★ 1.0k
0
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1
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4.3k
views
Comment: C: Is it 100% correct to transform SNP data (categorical) to (0, 1, 2) format to ap
7.8 years ago by Floris Brenk ★ 1.0k
1
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0
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5.9k
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Comment: C: Plink MDS plot based on IBS to exclude samples
7.8 years ago by Floris Brenk ★ 1.0k
0
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1
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5.9k
views
Comment: C: Plink MDS plot based on IBS to exclude samples
7.8 years ago by Floris Brenk ★ 1.0k
0
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0
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2.1k
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Comment: C: RNA-seq de novo transcript assembly from one gene
8.0 years ago by Floris Brenk ★ 1.0k
0
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1
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2.1k
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Comment: C: RNA-seq de novo transcript assembly from one gene
8.0 years ago by Floris Brenk ★ 1.0k
0
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1
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2.1k
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Comment: C: RNA-seq de novo transcript assembly from one gene
8.0 years ago by Floris Brenk ★ 1.0k
0
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0
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1.8k
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Comment: C: Coverage/Read Depth per SNP in 1000Genomes
8.0 years ago by Floris Brenk ★ 1.0k
0
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1
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2.8k
views
Comment: C: why is this example homozygous 0/0 ?
8.1 years ago by Floris Brenk ★ 1.0k
0
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0
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5.8k
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Comment: C: Convert Plink's ped file into compound genotype format and 0/1/2 format
8.1 years ago by Floris Brenk ★ 1.0k
0
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1
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5.8k
views
Comment: C: Convert Plink's ped file into compound genotype format and 0/1/2 format
8.1 years ago by Floris Brenk ★ 1.0k
1
vote
1
reply
5.8k
views
Comment: C: Convert Plink's ped file into compound genotype format and 0/1/2 format
8.1 years ago by Floris Brenk ★ 1.0k
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