Comparison of structural variations from 10X Genomics linked-reads and conventional Illumina short-reads sequencing
|Study ID||Alternative Stable ID||Type|
Study Datasets 1 dataset.
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This dataset contains whole genome sequencing data from Illumina short-reads sequencing (2X150bp) and 10X Genomics linked-reads sequencing. Both the sequencing technologies were used to sequence MCF7 cell line and a primary breast triple-negative cancer sample. The fastq of paired-end reads for both the samples sequenced with both the technologies is available.
|Illumina NovaSeq 6000||4|