NGS Details (SRR3458562_Metagenome_example): Sinsheimervirus phiX174

Assembly

1841 (9 contig(s))
1.2
17
1.10 rpm (after QC)
0
de novo + reference guided assembly
Bcf Tools

Coverage Map

Variant Tables

Assignment

Sinsheimervirus phiX174 (Taxonomy ID: 10847)
98.5877
95.8025
5
11

Alignment

3578.0 (NT) + 5217.0 (AA) = 8795.0
97.3221
Global, seeded, nucleotide + amino acids (AGA)

Alignment Detailed Statistics

BeginEndCoverageScoreConcordanceMatchesIdentitiesI/D/M/F*Stop Codons
NT751538634.2%357897.2%1841 (100%)1815 (98.6%)0/0
Mutations:
833G>A 934T>G 953C>A 1600T>A 1624A>C 2932T>G 2934T>C 2936T>G 2938G>C 2940G>A 2942T>G 2946G>A 2948T>A 2951C>G 2967C>G 2972T>C 2981C>A 2984G>A 2985T>A 3028T>C 3133C>T 3814T>G 4277A>T 4964A>C 5017A>C 5344T>G
CDS
146943.2%141995.9%222 (100%)215 (96.8%)0/0/0/00
Protein mutations:
K328N (4964A>C) K346T (5017A>C) F455C (5344T>G)
Codon mutations:
GCA99GCT (4277A>T) AAA328AAC (4964A>C) AAA346ACA (5017A>C) TTT455TGT (5344T>G)
13729735.7%73593.3%122 (100%)116 (95.1%)0/0/0/00
Protein mutations:
K156N (4964A>C) K174T (5017A>C) F283C (5344T>G)
Codon mutations:
AAA156AAC (4964A>C) AAA174ACA (5017A>C) TTT283TGT (5344T>G)
210462.8%54695.8%76 (100%)74 (97.4%)0/0/0/00
Protein mutations:
I90M (5344T>G)
Codon mutations:
ATT90ATG (5344T>G)
12215320.9%19295.0%32 (100%)32 (100%)0/0/0/01
629233.7%19697.5%31 (100%)30 (96.8%)0/0/0/01
Protein mutations:
R89Q (833G>A)
Codon mutations:
CGG89CAG (833G>A)
139100%26597.1%39 (100%)38 (97.4%)0/0/0/01
Protein mutations:
Q36K (953C>A)
Codon mutations:
CGT29CGG (934T>G) CAA36AAA (953C>A)
14038339.5%118496.3%169 (100%)165 (97.6%)0/0/0/01
Protein mutations:
Y200* (1600T>A) E208D (1624A>C)
Codon mutations:
TAT200TAA (1600T>A) GAA208GAC (1624A>C)
132936.2%68089.8%119 (100%)106 (89.1%)0/0/0/01
Protein mutations:
M1R (2932T>G) F2L (2934T>C 2936T>G) G3A (2938G>C) A4T (2940G>A 2942T>G) A6T (2946G>A 2948T>A) L13V (2967C>G) M18I (2984G>A) S19T (2985T>A) I33T (3028T>C) A68V (3133C>T) V295G (3814T>G)
Codon mutations:
ATG1AGG (2932T>G) TTT2CTG (2934T>C 2936T>G) GGT3GCT (2938G>C) GCT4ACG (2940G>A 2942T>G) GCT6ACA (2946G>A 2948T>A) GGC7GGG (2951C>G) CTT13GTT (2967C>G) GCT14GCC (2972T>C) GCC17GCA (2981C>A) ATG18ATA (2984G>A) TCT19ACT (2985T>A) ATT33ACT (3028T>C) GCC68GTC (3133C>T) GTT295GGT (3814T>G)
Proteins
146943.2%141995.9%222 (100%)215 (96.8%)0/0/0/00
Protein mutations:
K328N (4964A>C) K346T (5017A>C) F455C (5344T>G)
Codon mutations:
GCA99GCT (4277A>T) AAA328AAC (4964A>C) AAA346ACA (5017A>C) TTT455TGT (5344T>G)
13729735.7%73593.3%122 (100%)116 (95.1%)0/0/0/00
Protein mutations:
K156N (4964A>C) K174T (5017A>C) F283C (5344T>G)
Codon mutations:
AAA156AAC (4964A>C) AAA174ACA (5017A>C) TTT283TGT (5344T>G)
210462.8%54695.8%76 (100%)74 (97.4%)0/0/0/00
Protein mutations:
I90M (5344T>G)
Codon mutations:
ATT90ATG (5344T>G)
12215320.9%19295.0%32 (100%)32 (100%)0/0/0/01
Protein mutations:none
Codon mutations:
GCG148GCA (833G>A)
629233.7%19697.5%31 (100%)30 (96.8%)0/0/0/01
Protein mutations:
R89Q (833G>A)
Codon mutations:
CGG89CAG (833G>A)
139100%26597.1%39 (100%)38 (97.4%)0/0/0/01
Protein mutations:
Q36K (953C>A)
Codon mutations:
CGT29CGG (934T>G) CAA36AAA (953C>A)
14038339.5%118496.3%169 (100%)165 (97.6%)0/0/0/01
Protein mutations:
Y200* (1600T>A) E208D (1624A>C)
Codon mutations:
TAT200TAA (1600T>A) GAA208GAC (1624A>C)
132936.2%68089.8%119 (100%)106 (89.1%)0/0/0/01
Protein mutations:
M1R (2932T>G) F2L (2934T>C 2936T>G) G3A (2938G>C) A4T (2940G>A 2942T>G) A6T (2946G>A 2948T>A) L13V (2967C>G) M18I (2984G>A) S19T (2985T>A) I33T (3028T>C) A68V (3133C>T) V295G (3814T>G)
Codon mutations:
ATG1AGG (2932T>G) TTT2CTG (2934T>C 2936T>G) GGT3GCT (2938G>C) GCT4ACG (2940G>A 2942T>G) GCT6ACA (2946G>A 2948T>A) GGC7GGG (2951C>G) CTT13GTT (2967C>G) GCT14GCC (2972T>C) GCC17GCA (2981C>A) ATG18ATA (2984G>A) TCT19ACT (2985T>A) ATT33ACT (3028T>C) GCC68GTC (3133C>T) GTT295GGT (3814T>G)
*: Inserts / Deletes / Misaligned / Frameshifts

Analysis details

This analysis was performed with panviral2.43