NGS Details (SRR3458562_Metagenome_example): Friend murine leukemia virus

Assembly

280 (2 contig(s))
2.1
5
0.32 rpm (after QC)
0
de novo + reference guided assembly
Bcf Tools

Coverage Map

Variant Tables

Assignment

Friend murine leukemia virus (Taxonomy ID: 11795)
75.0903
79.5699
0
3

Alignment

266.0 (NT) + 511.0 (AA) = 777.0
67.7419
Global, seeded, nucleotide + amino acids (AGA)

Alignment Detailed Statistics

BeginEndCoverageScoreConcordanceMatchesIdentitiesI/D/M/F*Stop Codons
NT523375833.4%26649.1%277 (98.9%)208 (74.3%)0/3
Mutations:
5235T>C 5244A>G 5259T>A 5268A>G 5271A>G 5278A>C 5283A>C 5284A>T 5286C>A 5289G>A 5295T>C 5310G>T 5311C>A 5313T>G 5315C>A 5316A>G 5323T>G 5326_5328delAGG 5329G>A 5331C>T 5338C>G 5343G>T 5346T>C 5350C>T 5351T>A 5352A>C 5355C>T 5360A>T 5361T>C 5362C>G 5364A>G 5370C>T 5376G>C 7454A>G 7457G>A 7460A>C 7463A>G 7466G>C 7472T>A 7478A>C 7485G>C 7493T>C 7496C>T 7499T>C 7502T>A 7509A>T 7514C>A 7515C>G 7517A>G 7520A>T 7522G>A 7527A>T 7528G>C 7535C>A 7539T>C 7547G>A 7551C>T 7553C>A 7554T>G 7555C>A 7556T>C 7557C>A 7559G>A 7560A>C 7563C>A 7569C>G 7570T>A 7572T>A 7573T>G 7574T>A
CDS
100510534.1%25883.0%48 (98.0%)38 (77.6%)0/1/0/00
Protein mutations:
I1022L (5284A>T 5286C>A) L1031M (5311C>A 5313T>G) A1032E (5315C>A 5316A>G) S1035A (5323T>G) R1036del (5326_5328delAGG) D1037N (5329G>A 5331C>T) L1040V (5338C>G) L1044Y (5350C>T 5351T>A 5352A>C) Y1047F (5360A>T 5361T>C) R1048G (5362C>G 5364A>G)
Codon mutations:
TGT1005TGC (5235T>C) AGA1008AGG (5244A>G) GGT1013GGA (5259T>A) GAA1016GAG (5268A>G) AGA1017AGG (5271A>G) AGG1020CGG (5278A>C) ACA1021ACC (5283A>C) ATC1022TTA (5284A>T 5286C>A) AAG1023AAA (5289G>A) ACT1025ACC (5295T>C) ACG1030ACT (5310G>T) CTT1031ATG (5311C>A 5313T>G) GCA1032GAG (5315C>A 5316A>G) TCT1035GCT (5323T>G) AGG1036del (5326_5328delAGG) GAC1037AAT (5329G>A 5331C>T) CTC1040GTC (5338C>G) CTG1041CTT (5343G>T) CTT1042CTC (5346T>C) CTA1044TAC (5350C>T 5351T>A 5352A>C) GCC1045GCT (5355C>T) TAT1047TTC (5360A>T 5361T>C) CGA1048GGG (5362C>G 5364A>G) CGC1050CGT (5370C>T) ACG1052ACC (5376G>C)
5596036.6%25382.7%45 (100%)36 (80.0%)0/0/0/00
Protein mutations:
E571Q (7485G>C) T579S (7509A>T) L581V (7515C>G 7517A>G) R583K (7522G>A) S594D (7554T>G 7555C>A 7556T>C) Q595K (7557C>A 7559G>A) Q597K (7563C>A) L599E (7569C>G 7570T>A) F600R (7572T>A 7573T>G 7574T>A)
Codon mutations:
AAA560AAG (7454A>G) GAG561GAA (7457G>A) GGA562GGC (7460A>C) GGA563GGG (7463A>G) CTG564CTC (7466G>C) GCT566GCA (7472T>A) CTA568CTC (7478A>C) GAA571CAA (7485G>C) TGT573TGC (7493T>C) TTC574TTT (7496C>T) TAT575TAC (7499T>C) GCT576GCA (7502T>A) ACA579TCA (7509A>T) GGC580GGA (7514C>A) CTA581GTG (7515C>G 7517A>G) GTA582GTT (7520A>T) AGA583AAA (7522G>A) AGT585TCT (7527A>T 7528G>C) GCC587GCA (7535C>A) TTA589CTA (7539T>C) GAG591GAA (7547G>A) CTC593TTA (7551C>T 7553C>A) TCT594GAC (7554T>G 7555C>A 7556T>C) CAG595AAA (7557C>A 7559G>A) AGA596CGA (7560A>C) CAA597AAA (7563C>A) CTA599GAA (7569C>G 7570T>A) TTT600AGA (7572T>A 7573T>G 7574T>A)
Proteins
100510534.1%25883.0%48 (98.0%)38 (77.6%)0/1/0/00
Protein mutations:
I1022L (5284A>T 5286C>A) L1031M (5311C>A 5313T>G) A1032E (5315C>A 5316A>G) S1035A (5323T>G) R1036del (5326_5328delAGG) D1037N (5329G>A 5331C>T) L1040V (5338C>G) L1044Y (5350C>T 5351T>A 5352A>C) Y1047F (5360A>T 5361T>C) R1048G (5362C>G 5364A>G)
Codon mutations:
TGT1005TGC (5235T>C) AGA1008AGG (5244A>G) GGT1013GGA (5259T>A) GAA1016GAG (5268A>G) AGA1017AGG (5271A>G) AGG1020CGG (5278A>C) ACA1021ACC (5283A>C) ATC1022TTA (5284A>T 5286C>A) AAG1023AAA (5289G>A) ACT1025ACC (5295T>C) ACG1030ACT (5310G>T) CTT1031ATG (5311C>A 5313T>G) GCA1032GAG (5315C>A 5316A>G) TCT1035GCT (5323T>G) AGG1036del (5326_5328delAGG) GAC1037AAT (5329G>A 5331C>T) CTC1040GTC (5338C>G) CTG1041CTT (5343G>T) CTT1042CTC (5346T>C) CTA1044TAC (5350C>T 5351T>A 5352A>C) GCC1045GCT (5355C>T) TAT1047TTC (5360A>T 5361T>C) CGA1048GGG (5362C>G 5364A>G) CGC1050CGT (5370C>T) ACG1052ACC (5376G>C)
5596036.6%25382.7%45 (100%)36 (80.0%)0/0/0/00
Protein mutations:
E571Q (7485G>C) T579S (7509A>T) L581V (7515C>G 7517A>G) R583K (7522G>A) S594D (7554T>G 7555C>A 7556T>C) Q595K (7557C>A 7559G>A) Q597K (7563C>A) L599E (7569C>G 7570T>A) F600R (7572T>A 7573T>G 7574T>A)
Codon mutations:
AAA560AAG (7454A>G) GAG561GAA (7457G>A) GGA562GGC (7460A>C) GGA563GGG (7463A>G) CTG564CTC (7466G>C) GCT566GCA (7472T>A) CTA568CTC (7478A>C) GAA571CAA (7485G>C) TGT573TGC (7493T>C) TTC574TTT (7496C>T) TAT575TAC (7499T>C) GCT576GCA (7502T>A) ACA579TCA (7509A>T) GGC580GGA (7514C>A) CTA581GTG (7515C>G 7517A>G) GTA582GTT (7520A>T) AGA583AAA (7522G>A) AGT585TCT (7527A>T 7528G>C) GCC587GCA (7535C>A) TTA589CTA (7539T>C) GAG591GAA (7547G>A) CTC593TTA (7551C>T 7553C>A) TCT594GAC (7554T>G 7555C>A 7556T>C) CAG595AAA (7557C>A 7559G>A) AGA596CGA (7560A>C) CAA597AAA (7563C>A) CTA599GAA (7569C>G 7570T>A) TTT600AGA (7572T>A 7573T>G 7574T>A)
*: Inserts / Deletes / Misaligned / Frameshifts

Analysis details

This analysis was performed with panviral2.43