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Comment: Conflicting sequences between Genome Browser and NCBI (reference hg19).
15 months ago by
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Comment: DNA sequencing from cord blood stem cells
21 months ago by
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C: Best tool for variant calling
3.9 years ago by
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C: Retrieving multiple regions (from a list) in a bam file and outputing as a table
4.1 years ago by
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C: Run RNA-seq analysis with selected targets
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C: How to perform iteration task inside a docker image (RNA-seq analysis)
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C: How to compare sequencing data from same sample, but from different methods?
4.3 years ago by
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C: How to use ExAC/gnomAD without chrN_random?
4.4 years ago by
dodausp
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C: How to use ExAC/gnomAD without chrN_random?
4.4 years ago by
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C: How to skip vep-annotating step for vcf2maf
4.5 years ago by
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C: Infer somatic mutations without normal control
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C: Infer somatic mutations without normal control
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C: Infer somatic mutations without normal control
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C: Infer somatic mutations without normal control
4.6 years ago by
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C: Infer somatic mutations without normal control
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C: Infer somatic mutations without normal control
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C: Complex heatmaps: how not to cluster the slices?
4.6 years ago by
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C: How to Install SamTools, HTSLib, and BCFTools on Ubuntu 18.04
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C: Exploring association between genes by their expression
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A: Exploring association between genes by their expression
4.9 years ago by
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C: Exploring association between genes by their expression
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C: Exploring association between genes by their expression
5.0 years ago by
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C: Exploring association between genes by their expression
5.0 years ago by
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C: Extracting a specific string pattern from a list of objects
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C: Extracting a specific string pattern from a list of objects
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