Article

FINDEL: A Deep Learning Approach to Efficient Artifact Removal From Cancer Genomes

2022-11-14

Abstract excerpt

Next-generation sequencing technologies have increased sequencing throughput by 100-1000 folds and subsequently reduced the cost of sequencing a human genome to approximately US$1,000. However, the existence of sequencing artifacts can cause erroneous identification of variants and adversely impact the downstream analyses. Currently, the manual inspection of variants for additional refinement is still necessary fo...

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Literature Corpus work: ae5f4eba-e940-59cd-8eb5-bc539c2af12f
DOI: 10.1101/2022.11.12.516244

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