HRGF-GapCloser: A gap filling method base on HiFi read and read clustering

Author:

Shen Jiquan1ORCID,Liu Gang1ORCID,Luo Junwei1ORCID

Affiliation:

1. School of Software, Henan Polytechnic University, China

Funder

Young Backbone Teachers of Henan Province

Innovative Research Team of Henan Polytechnic University

Publisher

ACM

Reference30 articles.

1. PGcloser: fast parallel gap-closing tool using long-reads or contigs to fill gaps in genomes;Lu P;Evol. Bioinf.,2020

2. The SAMBA tool uses long reads to improve the contiguity of genome assemblies PLoS;Zimin AV;Comput. Biol.,2022

3. Lang D 2020. Comparison of the two up-to-date sequencing technologies for genome assembly: HiFi reads of Pacific Biosciences Sequel II system and ultralong reads of Oxford Nanopore Gigascience. 9 12 giaa123. https://academic.oup.com/gigascience/article/9/12/giaa123/6034784

4. Highly accurate long-read HiFi sequencing data for five complex genomes;Hon T;Sci. Data.,2020

5. HiFiAdapterFilt, a memory efficient read processing pipeline, prevents occurrence of adapter sequence in PacBio HiFi reads and their negative impacts on genome assembly BMC;Sim SB;Genomics.,2022

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