Distribution of mapped reads, bases, coverage and variants per sample.
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https://figshare.com/articles/dataset/_Distribution_of_mapped_reads_bases_coverage_and_variants_per_sample_/436114
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Distribution of mapped reads, bases, coverage and single nucleotide variants (SNVs) across the ten multiplex enriched breast cancer tumor samples. An even distribution across all samples except those tagged with multiplex identifier tag 3 and 9. Poor amplification characteristics of MID 3 was later verified by qPCR [21] to be the reason for poor representation of the corresponding sample among the sequence reads. The sample tagged with MID 9 was added in a lower molar amount upon pooling due to a low DNA concentration after library preparation.
创建时间：
2011-06-15
