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Comment: Comment: bcftools to remove non-variants sites
updated 4 months ago by 146k • written 4 months ago by • 0
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1.6k
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Comment: Comment: PLINK p value returning NA
6 months ago by Jingjingzhang • 0
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Answer: Answer: How to remove variants with 3+ alleles present Plink1.9
7 months ago by Jingjingzhang • 0
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32k
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Answer: Answer: How To Get Chromosome Position Given Rs Number?
updated 11 months ago by 146k • written 11 months ago by • 0
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2.2k
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Comment: Comment: looking for tools to detect RNA contamination in DNA
12 months ago by Jingjingzhang • 0
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2.0k
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Answer: Answer: filter multisample VCF based on Altered AD values
12 months ago by Jingjingzhang • 0
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4.1k
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Comment: Comment: Insert size is so small, good or bad?
14 months ago by Jingjingzhang • 0
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18k
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Comment: Comment: featureCounts strand specificity
2.2 years ago by Jingjingzhang • 0
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18k
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Comment: Comment: featureCounts strand specificity
2.2 years ago by Jingjingzhang • 0
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4.5k
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Answer: Answer: HIsat2 bam and summary output - multiple output file type
2.8 years ago by Jingjingzhang • 0
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2.2k
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Comment: C: Procedure to run OptiType for HLA Typing a BAM File
4.0 years ago by Jingjingzhang • 0
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810
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Is there any software or script to evaluate the accuracy of genotype imputation? Thanks!
genotype imputation gwas accuracy
4.5 years ago by Jingjingzhang • 0
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2.9k
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Comment: C: How to merge multiple CNV results of CNVnator
5.3 years ago by Jingjingzhang • 0
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6.5k
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Comment: C: Converting PLINK to EIGENSTRAT error using convertf (no valid snps)
5.9 years ago by Jingjingzhang • 0
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