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Sanger sequencing data to find the enriched SNV
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2020-06-22
相关数据集
A framework for the estimation of the proportion of true discoveries in single nucleotide variant detection studies for human data
Any single nucleotide variant detection study could benefit from a fast and cheap method of measuring the quality of variant call list. It is advantageous to be able to see how the call list quality i
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Detection of single nucleotide variations in expressed exons of the human genome using RNA-Seq
Whole genome re-sequencing is still a costly method to detect genetic mutations that lead to altered forms of proteins and may be associated with disease development. Since the majority of disease-rel
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Additional file 4: of QQ-SNV: single nucleotide variant detection at low frequency by comparing the quality quantiles
QQ-SNV. The ZIP archive contains the following three files: the main perl script file to be executed QQ-SNV_workflow.pl and the SAS files QQ-SNV.sas and get_quantiles.sas. To test QQ-SNV, the read ali
DataCite Commons2024-12-13 更新70
Additional file 7: of Dynamic transcriptome profiling of Bean Common Mosaic Virus (BCMV) infection in Common Bean (Phaseolus vulgaris L.)
Variants from BCMVS2 reads on the NL1I genome assembly. Variant-call-format file, showing single-nucleotide variants between the BCMVS2 genomic reads and the NL1I genome assembly. (ZIP 13Â kb)
Mendeley Data2024-06-28 更新60
