User: srmeetd

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Why might a large number of variants fail HWE?
... Hello everyone, Using RNA-seq sequence to genotype known variants. I have used the following steps: - GATK Haplotypecaller for variant calling - Filtering possible RNA editing events. - freebayes: Genotypes for the population at each position in the reference to get the homozygous reference. ...
snp rna-seq genome written 9 weeks ago by srmeetd0 • updated 8 weeks ago by i.sudbery10k

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