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Comment: Comment: UK Biobank Whole Exome Sequencing Homozygous Reference Positions
2.9 years ago by 4galaxy77 2.9k
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1.6k
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Answer: Answer: Confused about PED and MAP file
2.9 years ago by 4galaxy77 2.9k
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708
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Comment: Comment: signature of selection
2.9 years ago by 4galaxy77 2.9k
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796
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Comment: Comment: Recalculate R2 in imputed genotype data
2.9 years ago by 4galaxy77 2.9k
2
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1
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791
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Answer: Answer: The judgement of TP between the vcf files using vcfeval. Are 0/1 and 1/0 the sam
2.9 years ago by 4galaxy77 2.9k
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1
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827
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Comment: Comment: Phasing a partly-phased VCF
2.9 years ago by 4galaxy77 2.9k
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1
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1.0k
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Comment: Comment: GLIMPSE imputation result
2.9 years ago by 4galaxy77 2.9k
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2
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2.4k
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Comment: Comment: Legend and hap files for imputation with 38 build
2.9 years ago by 4galaxy77 2.9k
1
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1
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2.4k
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Comment: Comment: Legend and hap files for imputation with 38 build
2.9 years ago by 4galaxy77 2.9k
1
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1
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2.4k
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Comment: Comment: Legend and hap files for imputation with 38 build
2.9 years ago by 4galaxy77 2.9k
1
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1
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2.4k
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Comment: Comment: Legend and hap files for imputation with 38 build
2.9 years ago by 4galaxy77 2.9k
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0
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1.1k
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Comment: Comment: Keeping Only Informative SNPs
2.9 years ago by 4galaxy77 2.9k
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1
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1.1k
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Comment: Comment: Keeping Only Informative SNPs
2.9 years ago by 4galaxy77 2.9k
1
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0
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3.0k
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Comment: Comment: How to extract specific field from VCF?
2.9 years ago by 4galaxy77 2.9k
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2
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1.9k
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Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
3.0 years ago by 4galaxy77 2.9k
0
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1
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1.9k
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Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
3.0 years ago by 4galaxy77 2.9k
1
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0
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800
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Comment: Comment: vcftools- extract allele frequencies from pooled samples on a sample by sample b
3.0 years ago by 4galaxy77 2.9k
0
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0
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884
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Comment: Comment: PCA troubles
3.0 years ago by 4galaxy77 2.9k
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1
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1.2k
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Comment: Comment: Hide column label of genes
3.0 years ago by 4galaxy77 2.9k
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0
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1.2k
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Comment: Comment: Gwas Help.
3.0 years ago by 4galaxy77 2.9k
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1
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1.2k
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Comment: Comment: Gwas Help.
3.0 years ago by 4galaxy77 2.9k
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0
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2.0k
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Comment: Comment: How to add a individuals IDs to admixture output?
3.0 years ago by 4galaxy77 2.9k
1
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1
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1.3k
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Comment: Comment: Run Linux Commands and Scripts through R Studio terminal
3.0 years ago by 4galaxy77 2.9k
1
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1
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1.6k
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Answer: Answer: BAM dataset to Genotype data conversion using PLINK
3.0 years ago by 4galaxy77 2.9k
0
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1
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1.7k
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Comment: Comment: SHAPEIT using VCF unphased genotype input
3.0 years ago by 4galaxy77 2.9k
0
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1
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1.3k
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Comment: Comment: Bash loop, count for Chromopainter script
3.0 years ago by 4galaxy77 2.9k
1
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0
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1.5k
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Comment: Comment: Picard vs Samtools converting CRAM to FASTQ
3.0 years ago by 4galaxy77 2.9k
0
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1
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1.3k
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Answer: Answer: Bash loop, count for Chromopainter script
3.0 years ago by 4galaxy77 2.9k
0
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1
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1.3k
views
Answer: Answer: Phasing with Beagle 5.2 and no reference panel
3.0 years ago by 4galaxy77 2.9k
0
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1
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1.4k
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Comment: Comment: How to make .ped and .map files
3.0 years ago by 4galaxy77 2.9k
1
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1
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1.3k
views
Answer: Answer: Subsetting/filtering a tibble by a combination of data stored in a second tibble
3.0 years ago by 4galaxy77 2.9k
0
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0
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578
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Comment: Comment: I have genomic file. But it has different representation than usual
3.1 years ago by 4galaxy77 2.9k
1
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0
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844
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Comment: Comment: How can I obtain genotypes from .bams of RNAseq data?
3.1 years ago by 4galaxy77 2.9k
3
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1
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6.8k
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Answer: Answer: Should I buy a new apple M1-max with 64Gb Ram for single cell RNA seq analysis?
3.1 years ago by 4galaxy77 2.9k
1
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0
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15k
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Comment: Comment: How to convert a bcf file to vcf with bcftools?
3.1 years ago by 4galaxy77 2.9k
2
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1
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15k
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Answer: Answer: How to convert a bcf file to vcf with bcftools?
3.1 years ago by 4galaxy77 2.9k
1
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1
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1.2k
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Answer: Answer: Speeding up Eagle phasing and imputation
3.1 years ago by 4galaxy77 2.9k
1
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0
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2.4k
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Answer: Answer: Sliding window plot using Python
3.1 years ago by 4galaxy77 2.9k
0
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0
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2.1k
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Comment: Comment: ABBA BABA test for two population
3.1 years ago by 4galaxy77 2.9k
3
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1
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1.2k
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Answer: Answer: Filtering with vcftools by QUAL, Does not produce an output file
3.1 years ago by 4galaxy77 2.9k
0
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0
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1.6k
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Comment: Comment: New datasets for ancestry estimation and imputation?
3.1 years ago by 4galaxy77 2.9k
0
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0
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802
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Answer: Answer: vcf file indiviual column interpretation
3.1 years ago by 4galaxy77 2.9k
0
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0
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1.5k
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Comment: Comment: How long does it take to carry out the GWAS workflow?
3.1 years ago by 4galaxy77 2.9k
2
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0
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2.2k
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Answer: Answer: Open source python tool for convert VCF files to JSON?
3.1 years ago by 4galaxy77 2.9k
0
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1
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1.0k
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Comment: Comment: How do I merge imputed GWAS data
3.1 years ago by 4galaxy77 2.9k
4
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1
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1.2k
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Answer: Answer: adding allele frequencies to a vcf
3.1 years ago by 4galaxy77 2.9k
1
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1
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1.6k
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Comment: Comment: How to convert multiple .vcf files into single .ped (PLINK compatible files)?
3.1 years ago by 4galaxy77 2.9k
1
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1
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1.4k
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Comment: Comment: Type of analyses Which can be performed on Whole Genome Data
3.2 years ago by 4galaxy77 2.9k
0
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0
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1.8k
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Comment: Comment: What current tools are used to phase haplotypes from a FASTQ file?
3.2 years ago by 4galaxy77 2.9k
0
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3
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1.8k
views
Comment: Comment: What current tools are used to phase haplotypes from a FASTQ file?
3.2 years ago by 4galaxy77 2.9k
439 results • Page 5 of 9
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