Copyright
©The Author(s) 2015.
World J Hepatol. Apr 28, 2015; 7(6): 831-845
Published online Apr 28, 2015. doi: 10.4254/wjh.v7.i6.831
Published online Apr 28, 2015. doi: 10.4254/wjh.v7.i6.831
Platform | Run time (h) | Read length (bp) | Throughput per run (Mb) | Typical errors | Main biological applications | Company URL |
Roche 454 FLX + | 23 | 700, up to 1000 | 700 | Insertions/deletions (indels) at homopolymer regions | Microbial genome sequencing, human genome sequencing, transcriptomics, metagenomics | http://www.my454.com/ |
Illumina HySeq 1000 MySeq 2000 V3 | 8 10 | 2 × 100 2 × 150 | 400000 < 600000 | Indels, especially end of reads | Microbial genome sequencing, human genome sequencing, transcriptomics, metagenomics | http://www.illumina.com/systems.ilmn |
SOLiD 4 | 12 | 50 × 35 | 71000 | End of read substitution errors | Microbial genome sequencing, human genome sequencing, transcriptomics, metagenomics | http://www.appliedbiosystems.com/ absite/us/en/home.html |
Ion torrent PGM 318 Chip | 3 | 200 | 1000 | Indels at homopolymer regions | Microbial genome sequencing, human genome sequencing, transcriptomics, metagenomics | http://www.iontorrent.com/ |
Pacific Biosciences | Random indel errors | Full-length transcriptomics, discovering large structural variants and haplotypes | http://www.pacificbiosciences.com/ |
Strain | Genotype | Country | Recombination breakpoint(s) | Ref. |
Intergenotype | ||||
RF1_2k/1b | 2k/1b | Russia, Ireland, Uzbekistan, Georgia, France, Cyprus, Estonia | NS2, positions 3175-3176 | [124-129] |
D3 | 2i/6p | Viet Nam | NS2/NS3 junction, between positions 3405 and 3464 | [130] |
SE-03-07-1689 | RF3_2b/1b | Philippines | NS3, positions 3466-3467 | [137] |
HC10-0804 | 2b/1b | Japan | NS2/NS3 junction, positions 3443-3444 | [135] |
B5808, M2123, M4430, M4416, M4414, M4431, M2777, M8774 | 2b/1b | Japan | NS2, putative position 3301 | [136] |
R1 | 2/5 | France | NS2/NS3 junction, between residues 3420 and 3440 | [132] |
D177 | RF_2b/6w RF_3a/1b RF_2a/1a | Taiwan Taiwan, China Taiwan | NS2/NS3 junction, position 3429 Undetermined Undetermined | [131,133] |
JF779679 | 2b/1a | United States | NS2/NS3 junction, positions 3405-3416 | [134] |
Intersubtype | Subtypes | |||
PE22 | RF2_1b/1a | Peru | NS5B, position 8321 | [141] |
H23 | 1b/1a | Uruguay | Core, at position 387 | [111] |
HC-J1 | 1a/1c | Japan | 2 sites in E1-E2, at positions 1407 and 2050 | [142] |
Khajal | 1a/1c | India | 5 sites, from core to NS3, at positions 801 1261, 2181, 3041 and 3781 | [143] |
R49 | 4a/4d | Portugal | Undetermined | [140] |
EU246930 | 6a/6o | Viet Nam | NS5B, between positions 8345-9073 | [144] |
EU246932 | 6e/6o | Viet Nam | NS5B, between positions 8358-8977 | [144] |
EU246937 | 6n/6o | Thailand | NS5B, between positions 8372-9033 | [144] |
EU246931 | 6e/6h | Viet Nam | NS5B, between positions 8356-9019 | [144] |
Intrapatient | Subtype | |||
1b | Spain | NS5B, at residue 286 | [145] | |
1a, 1b, 3a | Spain | 1 or 2 sites within E1-E2 or NS5A | [146] | |
4a | Ireland | E2 glycoprotein, HVR1 region | [147] |
- Citation: Echeverría N, Moratorio G, Cristina J, Moreno P. Hepatitis C virus genetic variability and evolution. World J Hepatol 2015; 7(6): 831-845
- URL: https://www.wjgnet.com/1948-5182/full/v7/i6/831.htm
- DOI: https://dx.doi.org/10.4254/wjh.v7.i6.831