Long Read Sequencing of Filaggrin identifies extensive copy number variation in the FLG repeat of exon 3 and detects rare loss of function variants
收藏NIAID Data Ecosystem2026-05-10 收录
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https://www.ncbi.nlm.nih.gov/sra/ERP179801
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资源简介：
Long-read sequencing data of 192 humans from Belgium, Ireland and Rwanda. Sequences have been obtained by PCR amplification of the FLG gene. Alignments are based on the hg19 reference (GRCh37).
创建时间：
2026-01-20
