NGS Details (ERR138007_norovirus_amplicon_example): Simian immunodeficiency virus

Assembly

137 (1 contig(s))
1.7
2
4.26 rpm (after QC)
2
de novo + reference guided assembly
Bcf Tools

Coverage Map

Variant Tables

Assignment

Simian immunodeficiency virus (Taxonomy ID: 11723)
78.1022
84.4444
0
6

Alignment

158.0 (NT) + 576.0 (AA) = 734.0
78.0851
Global, seeded, nucleotide + amino acids (AGA)

Alignment Detailed Statistics

BeginEndCoverageScoreConcordanceMatchesIdentitiesI/D/M/F*Stop Codons
NT145915951.4%15857.7%137 (100%)107 (78.1%)0/0
Mutations:
1466C>A 1471T>C 1472A>C 1480A>G 1481C>A 1484T>C 1487G>A 1493A>T 1500A>G 1502T>G 1503C>T 1505T>G 1514C>A 1517T>C 1523A>G 1535G>R 1541C>T 1544G>A 1547A>T 1550C>T 1551A>C 1552G>C 1557C>G 1560G>A 1561C>T 1562T>G 1565C>G 1568G>R 1575G>C 1592C>T
CDS
1892333.1%28884.5%45 (100%)38 (84.4%)0/0/0/00
Protein mutations:
V192A (1471T>C 1472A>C) D195G (1480A>G 1481C>A) I202V (1500A>G 1502T>G) R219P (1551A>C 1552G>C) P221A (1557C>G) A222M (1560G>A 1561C>T 1562T>G) A227P (1575G>C)
Codon mutations:
CTC190CTA (1466C>A) GTA192GCC (1471T>C 1472A>C) GAC195GGA (1480A>G 1481C>A) CAT196CAC (1484T>C) CAG197CAA (1487G>A) GCA199GCT (1493A>T) ATT202GTG (1500A>G 1502T>G) CTT203TTG (1503C>T 1505T>G) GTC206GTA (1514C>A) ATT207ATC (1517T>C) GAA209GAG (1523A>G) GAG213GAR (1535G>R) GAC215GAT (1541C>T) AGG216AGA (1544G>A) ACA217ACT (1547A>T) CAC218CAT (1550C>T) AGA219CCA (1551A>C 1552G>C) CCA221GCA (1557C>G) GCT222ATG (1560G>A 1561C>T 1562T>G) GGC223GGG (1565C>G) CCG224CCR (1568G>R) GCA227CCA (1575G>C) GAC232GAT (1592C>T)
1892338.8%28884.5%45 (100%)38 (84.4%)0/0/0/00
Protein mutations:
V192A (1471T>C 1472A>C) D195G (1480A>G 1481C>A) I202V (1500A>G 1502T>G) R219P (1551A>C 1552G>C) P221A (1557C>G) A222M (1560G>A 1561C>T 1562T>G) A227P (1575G>C)
Codon mutations:
CTC190CTA (1466C>A) GTA192GCC (1471T>C 1472A>C) GAC195GGA (1480A>G 1481C>A) CAT196CAC (1484T>C) CAG197CAA (1487G>A) GCA199GCT (1493A>T) ATT202GTG (1500A>G 1502T>G) CTT203TTG (1503C>T 1505T>G) GTC206GTA (1514C>A) ATT207ATC (1517T>C) GAA209GAG (1523A>G) GAG213GAR (1535G>R) GAC215GAT (1541C>T) AGG216AGA (1544G>A) ACA217ACT (1547A>T) CAC218CAT (1550C>T) AGA219CCA (1551A>C 1552G>C) CCA221GCA (1557C>G) GCT222ATG (1560G>A 1561C>T 1562T>G) GGC223GGG (1565C>G) CCG224CCR (1568G>R) GCA227CCA (1575G>C) GAC232GAT (1592C>T)
Proteins
1892333.1%28884.5%45 (100%)38 (84.4%)0/0/0/00
Protein mutations:
V192A (1471T>C 1472A>C) D195G (1480A>G 1481C>A) I202V (1500A>G 1502T>G) R219P (1551A>C 1552G>C) P221A (1557C>G) A222M (1560G>A 1561C>T 1562T>G) A227P (1575G>C)
Codon mutations:
CTC190CTA (1466C>A) GTA192GCC (1471T>C 1472A>C) GAC195GGA (1480A>G 1481C>A) CAT196CAC (1484T>C) CAG197CAA (1487G>A) GCA199GCT (1493A>T) ATT202GTG (1500A>G 1502T>G) CTT203TTG (1503C>T 1505T>G) GTC206GTA (1514C>A) ATT207ATC (1517T>C) GAA209GAG (1523A>G) GAG213GAR (1535G>R) GAC215GAT (1541C>T) AGG216AGA (1544G>A) ACA217ACT (1547A>T) CAC218CAT (1550C>T) AGA219CCA (1551A>C 1552G>C) CCA221GCA (1557C>G) GCT222ATG (1560G>A 1561C>T 1562T>G) GGC223GGG (1565C>G) CCG224CCR (1568G>R) GCA227CCA (1575G>C) GAC232GAT (1592C>T)
1892338.8%28884.5%45 (100%)38 (84.4%)0/0/0/00
Protein mutations:
V192A (1471T>C 1472A>C) D195G (1480A>G 1481C>A) I202V (1500A>G 1502T>G) R219P (1551A>C 1552G>C) P221A (1557C>G) A222M (1560G>A 1561C>T 1562T>G) A227P (1575G>C)
Codon mutations:
CTC190CTA (1466C>A) GTA192GCC (1471T>C 1472A>C) GAC195GGA (1480A>G 1481C>A) CAT196CAC (1484T>C) CAG197CAA (1487G>A) GCA199GCT (1493A>T) ATT202GTG (1500A>G 1502T>G) CTT203TTG (1503C>T 1505T>G) GTC206GTA (1514C>A) ATT207ATC (1517T>C) GAA209GAG (1523A>G) GAG213GAR (1535G>R) GAC215GAT (1541C>T) AGG216AGA (1544G>A) ACA217ACT (1547A>T) CAC218CAT (1550C>T) AGA219CCA (1551A>C 1552G>C) CCA221GCA (1557C>G) GCT222ATG (1560G>A 1561C>T 1562T>G) GGC223GGG (1565C>G) CCG224CCR (1568G>R) GCA227CCA (1575G>C) GAC232GAT (1592C>T)
*: Inserts / Deletes / Misaligned / Frameshifts

Analysis details

This analysis was performed with panviral2.43