Additional file 1: Table S1. of ScanIndel: a hybrid framework for indel detection via gapped alignment, split reads and de novo assembly
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https://figshare.com/articles/dataset/Additional_file_1_Table_S1_of_ScanIndel_a_hybrid_framework_for_indel_detection_via_gapped_alignment_split_reads_and_de_novo_assembly/4468820
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资源简介：
A list of 138 validated deletions from the literature and 105 previously predicted novel sequence insertions identified by the 1000 Genomes Projects for human NIST standard NA12878. The genome coordinates are mapped to hg19. (XLSX 18 kb)
创建时间：
2016-12-16
