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Comment: Comment: Need help understanding core SNPs
14 months ago by Prash ▴ 290
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Comment: Comment: Why are some WES VCFs larger than others?
24 months ago by Prash ▴ 290
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Comment: Comment: Pan genome based assembly
2.0 years ago by Prash ▴ 290
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Comment: Comment: How many basepairs are genes padded by in WES?
2.3 years ago by Prash ▴ 290
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Comment: Comment: Paired - end sequencing
2.4 years ago by Prash ▴ 290
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Comment: Comment: Advice on how to generate synthetic Copy Number Variation data
2.6 years ago by Prash ▴ 290
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2.3k
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Comment: Comment: NGS Sequence quality
2.6 years ago by Prash ▴ 290
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Comment: Comment: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
2.7 years ago by Prash ▴ 290
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4.5k
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Comment: Comment: Commercial software for genomics / NGS / bioinformatics
2.7 years ago by Prash ▴ 290
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4.9k
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Comment: Comment: How to filter SNPs with excess heterozygosity from a large vcf
2.8 years ago by Prash ▴ 290
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2.2k
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Comment: Comment: WES data analysis: the rationale behind merging BAM files and marking duplicates
3.1 years ago by Prash ▴ 290
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7.0k
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Comment: Comment: Error with per tile sequence quality (by FastQC)
3.1 years ago by Prash ▴ 290
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Comment: Comment: Variant Allele frequency
3.1 years ago by Prash ▴ 290
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1.8k
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Comment: Comment: When to merge BAM or SAM files?
3.2 years ago by Prash ▴ 290
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