Showing: variantcallingreset
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VariantCalling with single sanger read
indel snps variantcalling blast written 2.9 years ago by Amirosein70 • updated 5 months ago by trausch1.3k
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CRAM reference registry and the GRch38 reference genome
cram bam samtools variantcalling grch38 written 7 months ago by Mehulsharma.25310 • updated 7 months ago by h.mon26k
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GATK best practices for Broad-produced NGS data
gatk4 ngs broadinstitute variantcalling written 7 months ago by Mehulsharma.25310 • updated 7 months ago by vdauwera940
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Using the ranking value to filter
discosnp++ discosnp rna-seq variantcalling filter written 15 months ago by vguerracanedo10 • updated 15 months ago by pierre.peterlongo840
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Lowercase variants reported by SomaticSniper
somaticsniper variantcalling written 24 months ago by Inés Sentís10 • updated 24 months ago by Pierre Lindenbaum121k
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Intronic Variant Filtering
intron snp variantcalling written 2.0 years ago by cvu140 • updated 2.0 years ago by Samuel Brady300
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Variant calling for sanger reads
sanger alignment variantcalling variants written 2.9 years ago by Amirosein70 • updated 2.9 years ago by Keith Callenberg890
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Base Quality of a reported variant in VCF
vcf next-gen fastq alignment variantcalling written 4.4 years ago by VineethVenumadhavan30 • updated 4.4 years ago by Devon Ryan91k
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