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Comment: Comment: Mapping and annotation using the T2T-CHM13 reference genome
9 weeks ago by Jingjingzhang ▴ 10
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Comment: Comment: bcftools to remove non-variants sites
updated 10 months ago by 151k • written 10 months ago by ▴ 10
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Comment: Comment: PLINK p value returning NA
12 months ago by Jingjingzhang ▴ 10
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Answer: Answer: How to remove variants with 3+ alleles present Plink1.9
13 months ago by Jingjingzhang ▴ 10
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Answer: Answer: How To Get Chromosome Position Given Rs Number?
updated 17 months ago by 151k • written 17 months ago by ▴ 10
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Comment: Comment: looking for tools to detect RNA contamination in DNA
18 months ago by Jingjingzhang ▴ 10
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Answer: Answer: filter multisample VCF based on Altered AD values
18 months ago by Jingjingzhang ▴ 10
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Comment: Comment: Insert size is so small, good or bad?
20 months ago by Jingjingzhang ▴ 10
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Comment: Comment: featureCounts strand specificity
2.7 years ago by Jingjingzhang ▴ 10
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20k
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Comment: Comment: featureCounts strand specificity
2.7 years ago by Jingjingzhang ▴ 10
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Answer: Answer: HIsat2 bam and summary output - multiple output file type
3.3 years ago by Jingjingzhang ▴ 10
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Comment: C: Procedure to run OptiType for HLA Typing a BAM File
4.5 years ago by Jingjingzhang ▴ 10
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Is there any software or script to evaluate the accuracy of genotype imputation? Thanks!
genotype imputation gwas accuracy
5.0 years ago by Jingjingzhang ▴ 10
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Comment: C: How to merge multiple CNV results of CNVnator
5.8 years ago by Jingjingzhang ▴ 10
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Comment: C: Converting PLINK to EIGENSTRAT error using convertf (no valid snps)
6.4 years ago by Jingjingzhang ▴ 10
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