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Symphonizing pileup and full-alignment for deep learning-based long-read variant calling.

, , , , , and . Nat. Comput. Sci., 2 (12): 797-803 (2022)

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database.bio: a web application for interpreting human variations., , , , , , , , , and 1 other author(s). Bioinform., 31 (24): 4035-4037 (2015)MegaPath-Nano: Accurate Compositional Analysis and Drug-level Antimicrobial Resistance Detection Software for Oxford Nanopore Long-read Metagenomics., , , , , , , and . BIBM, page 329-336. IEEE, (2020)RENET: A Deep Learning Approach for Extracting Gene-Disease Associations from Literature., , , , and . RECOMB, volume 11467 of Lecture Notes in Computer Science, page 272-284. Springer, (2019)BioNumQA-BERT: answering biomedical questions using numerical facts with a deep language representation model., , , and . BCB, page 57:1-57:6. ACM, (2021)MC-Explorer: Analyzing and Visualizing Motif-Cliques on Large Networks., , , , , , , and . ICDE, page 1722-1725. IEEE, (2020)Large-scale Dataset and Effective Model for Variant-Disease Associations Extraction., , , , and . BCB, page 37:1-37:6. ACM, (2023)ChromSeg: Two-Stage Framework for Overlapping Chromosome Segmentation and Reconstruction., , , , and . BIBM, page 2335-2342. IEEE, (2020)Skyhawk: an artificial neural network-based discriminator for reviewing clinically significant genomic variants., , and . Int. J. Comput. Biol. Drug Des., 13 (5/6): 431-437 (2020)CellContrast: Reconstructing spatial relationships in single-cell RNA sequencing data via deep contrastive learning., , , , , , and . Patterns, 5 (8): 101022 (2024)FaSD-somatic: a fast and accurate somatic SNV detection algorithm for cancer genome sequencing data., , , , , , and . Bioinform., 30 (17): 2498-2500 (2014)