Comparison between MGI and Illumina sequencing platforms for whole genome sequencing

[1] Alioto TS(2015)A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing Nat Commun 6 10001-8

[2] Buchhalter I(2018)Assessment of the cPAS-based BGISEQ-500 platform for metagenomic sequencing Gigascience 7 1-2679

[3] Derdak S(2012)Qualimap: evaluating next-generation sequencing alignment data Bioinformatics 28 2678-351

[4] Hutter B(2016)Coming of age: ten years of next-generation sequencing technologies Nat Rev Genet 17 333-673

[5] Eldridge MD(2020)Comparative analysis of novel MGISEQ-2000 sequencing platform vs Illumina HiSeq 2500 for whole-genome sequencing PLoS One 15 e0230301-2079

[6] Hovig E(2019)Next-Generation Sequencing and Emerging Technologies Semin Thromb Hemost 45 661-1303

[7] Heisler LE(2009)The Sequence Alignment/Map format and SAMtools Bioinformatics 25 2078-undefined

[8] Beck TA(2010)The genome analysis toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data Genome Res 20 1297-undefined

[9] Simpson JT(2019)Comparative analysis of sequencing technologies for single-cell transcriptomics Genome Biol 20 70-undefined

[10] Tonon L(2018)Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing PLoS One 13 e0190264-undefined

[1] Alioto TS(2015)A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing Nat Commun 6 10001-8

[2] Buchhalter I(2018)Assessment of the cPAS-based BGISEQ-500 platform for metagenomic sequencing Gigascience 7 1-2679

[3] Derdak S(2012)Qualimap: evaluating next-generation sequencing alignment data Bioinformatics 28 2678-351

[4] Hutter B(2016)Coming of age: ten years of next-generation sequencing technologies Nat Rev Genet 17 333-673

[5] Eldridge MD(2020)Comparative analysis of novel MGISEQ-2000 sequencing platform vs Illumina HiSeq 2500 for whole-genome sequencing PLoS One 15 e0230301-2079

[6] Hovig E(2019)Next-Generation Sequencing and Emerging Technologies Semin Thromb Hemost 45 661-1303

[7] Heisler LE(2009)The Sequence Alignment/Map format and SAMtools Bioinformatics 25 2078-undefined

[8] Beck TA(2010)The genome analysis toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data Genome Res 20 1297-undefined

[9] Simpson JT(2019)Comparative analysis of sequencing technologies for single-cell transcriptomics Genome Biol 20 70-undefined

[10] Tonon L(2018)Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing PLoS One 13 e0190264-undefined