‘Fastq-to-Variants’ can align raw NGS sequencing data to the reference genome of 2019nCoV, identify 2019nCoV genetic sequences from the sequencing sample(s), analyze the degree of genomic coverage, sequencing depth, sequencing error rates, detect and annotate the SNPs or Indels.
Reference running time is tested using real data set when the server system is idle (not including upload time). Running time of actual tasks depend on the workload state of the server system, data volume, data quality and so on.
Data1 | Data2 | Data3 | Data4 | Data5 | |
Data Volume | 118Mb | 1.0Gb | 1.5Gb | 2.2Gb | 8.0Gb |
Calculating Time* | 0m37s | 0m55s | 1m10s | 1m36s | 3m42s |
Accession | SRR11247077 | SRR11092064 | SRR11092057 | SRR11092058 | SRR10971381 |
*Run on 24 CPU cores
This tool can detect mutation sites in the virus genome sequence. SARS-CoV-2 (NC_045512) and your upload fasta file are supported as reference for the online variation identification. The input file can be the whole genome sequence of virus(es) in the format of FASTA, and support for partial sequence(s) also.
You must upload single FASTA format file contain one virus genomic sequence or multiple sequences.
1). NC - Maximum number of N's contained in the input fasta sequence, the default value is 15, Discard the sequences when number of N's of genome greater than NC number;
2). SC - Maximum number of the degenerate bases contained in the input fasta sequence, the default value is 50, Discard the sequences when number of degenerate bases of genome greater than SC number;