Comparative analysis of 7 short-read sequencing platforms using the Korean Reference Genome: MGI and Illumina sequencing benchmark for whole-genome sequencing
Author(s) -
HakMin Kim,
Sungwon Jeon,
Oksung Chung,
Je Hoon Jun,
Hui-Su Kim,
Asta Blažytė,
Hwang-Yeol Lee,
Youngseok Yu,
Yun Sung Cho,
Dan Bolser,
Jong Bhak
Publication year - 2021
Publication title -
gigascience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.947
H-Index - 54
ISSN - 2047-217X
DOI - 10.1093/gigascience/giab014
Subject(s) - dbsnp , illumina dye sequencing , genotyping , genetics , genome , dna sequencing , biology , cancer genome sequencing , computational biology , reference genome , whole genome sequencing , genomics , personal genomics , massive parallel sequencing , single nucleotide polymorphism , genotype , gene
DNBSEQ-T7 is a new whole-genome sequencer developed by Complete Genomics and MGI using DNA nanoball and combinatorial probe anchor synthesis technologies to generate short reads at a very large scale-up to 60 human genomes per day. However, it has not been objectively and systematically compared against Illumina short-read sequencers.
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