2018
DOI: 10.1016/j.virol.2017.11.001
|View full text |Cite
|
Sign up to set email alerts
|

Discovery of novel anelloviruses in small mammals expands the host range and diversity of the Anelloviridae

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

0
40
0
1

Year Published

2018
2018
2023
2023

Publication Types

Select...
4
3
1

Relationship

3
5

Authors

Journals

citations
Cited by 53 publications
(41 citation statements)
references
References 47 publications
0
40
0
1
Order By: Relevance
“…Sequencing was performed at the Life Sciences Core Facility from University of Campinas, Brazil. The resulting sequencing reads were assembled de novo using the metaViC pipeline ( https://github.com/sejmodha/MetaViC ) 28 . This pipeline is divided into two major components.…”
Section: Methodsmentioning
confidence: 99%
“…Sequencing was performed at the Life Sciences Core Facility from University of Campinas, Brazil. The resulting sequencing reads were assembled de novo using the metaViC pipeline ( https://github.com/sejmodha/MetaViC ) 28 . This pipeline is divided into two major components.…”
Section: Methodsmentioning
confidence: 99%
“…Tissue samples were individually homogenized with Hank’s balanced salt solution using the TissueLyser system (Qiagen, Germantown, MD, USA). Then, the homogenized tissue, sera and cloacal swabs were centrifuged for 5 min at 10,000 g and the pools were prepared as previously described [ 12 ]. The viral genomes were extracted with a QIAamp viral RNA mini kit (Qiagen, USA) and stored at −80 °C.…”
Section: Methodsmentioning
confidence: 99%
“…A total of 7,059,398 to 94,508,748 paired-end reads per pool were generated with 64.85% to 91.45% of bases ≥ Q30 with a base call accuracy of 99.9% ( Table S1 ). The sequencing reads were assembled using the de novo approach in the metaViC pipeline ( ) [ 12 ]. The parvovirus contigs longer than length of 200 nucleotides and supercontigs were merged and classified using DIAMOND against NCBI RefSeq protein database [ 13 , 14 ].…”
Section: Methodsmentioning
confidence: 99%
“…Tissues samples were individually homogenized with Hank’s balanced salt solution using the TissueLyser system (Qiagen, USA). Then, the homogenized tissue, sera, and cloacal swabs were centrifuged by 5 min at 10,000g, and the pools were prepared as previously described [12]. The viral genomes were extracted with a QIAamp viral RNA mini kit (Qiagen, USA) and stored at −80°C.…”
Section: Methodsmentioning
confidence: 99%
“…A total of 7,059,398 to 94,508,748 paired-end reads per pool were generated with 64.85% to 91.45% of bases ≥ Q30 with a base call accuracy of 99.9% (Supplementary Table 1). The sequencing reads were assembled using the de novo approach in the metaViC pipeline (github.com/sejmodha/MetaViC) [12].…”
Section: Methodsmentioning
confidence: 99%