Strand-specific libraries were generated as previously described10 (link), from 192 barcoded single-cells and sequenced on a NextSeq Illumina platform. The 192 barcoded single-cell libraries were pooled for sequencing of the HG002 sample. Raw demultiplexed fastq files from the paired-end sequencing run (80-bp read lengths) were uploaded for each single-cell library. These data can be found at https://s3-us-west-2.amazonaws.com/human-pangenomics/index.html?prefix=HG002/hpp_HG002_NA24385_son_v1/Strand_seq/.
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