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Author: Alexander E. Urban

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  • All-time downloads: 21,124 (rank: 2,713 out of 396,038)
  • Categories:
    • bioinformatics: 4,452 (rank: 2,130 out of 33,633)
    • genetics: 2,201 (rank: 7,110 (tie) out of 36,269)
    • genomics: 14,471 (rank: 802 out of 42,088)

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Preprints

Highly sensitive and full-genome interrogation of SARS-CoV-2 using multiplexed PCR enrichment followed by next-generation sequencing

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Whole-genome sequencing analysis of copy number variation (CNV) using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis

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Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562

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Detection of complex structural variation from paired-end sequencing data

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Haplotype-resolved and integrated genome analysis of the cancer cell line HepG2

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Allele-specific binding of RNA-binding proteins reveals functional genetic variants in the RNA

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Local and global chromatin interactions are altered by large genomic deletions associated with human brain development

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Machine learning reveals bilateral distribution of somatic L1 insertions in human neurons and glia

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Extensive and deep sequencing of the Venter/HuRef genome for developing and benchmarking genome analysis tools

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Haplotype-phased common marmoset embryonic stem cells for genome editing using CRISPR/Cas9

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Network effects of the neuropsychiatric 15q13.3 microdeletion on the transcriptome and epigenome in human induced neurons

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Genome-wide molecular effects of the neuropsychiatric 16p11 CNVs in an iPSC-to-iN neuronal model

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Full-length LINE-1s with functional ORFs are favoured by host-level selection in human genomes

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