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WebBy mapping PacBio HiFi reads from the CHM13 cell line ( 27) as well as Illumina-like simulated reads (150 bp) obtained from the T2T-CHM13 reference to GRCh38, we identified 368,574 heterozygous SNVs within the autosomes and chromosome X, of which 56,413 (15.3%) were shared between datasets. WebApr 23, 2024 · Amparo Tolosa, Genética Médica News. El área de la Genética Médica y Medicina Genómica evoluciona sin descanso. Desde Genética Médica News, hacemos … the world fastest reader
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