Table S9 NCBI SARS-CoV-2 samples SNVs called during the first and second waves
Harvard Dataverse (Africa Rice Center, Bioversity International, CCAFS, CIAT, IFPRI, IRRI and WorldFish)
View Archive InfoField | Value | |
Title |
Table S9 NCBI SARS-CoV-2 samples SNVs called during the first and second waves
|
|
Identifier |
https://doi.org/10.7910/DVN/4ZXDW0
|
|
Creator |
N'Guessan, Arnaud
|
|
Publisher |
Harvard Dataverse
|
|
Description |
The table contains immunological, genomic and sequencing features of single nucleotide variants (SNVs) from 38,685 whole genome sequences from the NCBI sequence read archive. The SARS-CoV-2 samples from the first pandemic wave (defined as January 1 to July 31, 2020) and the second wave (defined as August 1 to December 31 2020) were sequenced using Illumina paired-end amplicons with a minimum average depth of coverage of 200 x and fewer than 10,000 sites with a depth of coverage lower than 100x. Additionally, we selected SNVs present in both minus and plus strands at a minimum frequency of 2%, occurring at sites with a minimum depth of 100x, having a minimum within-sample frequency of 5% and located between sites 101 and 29778 of the genome to exclude sites at the extremities that are prone to sequencing errors and have been frequently masked. |
|
Subject |
Medicine, Health and Life Sciences
|
|
Contributor |
N'Guessan, Arnaud
|
|