doc-ANNOVAR software on GitHub in support of 'Identification and Prioritisation of Variants in the Short Open-Reading Frame Regions of the Human Genome'

integration_instructionsResearch softwarekeyboard_double_arrow_right Software

doc-ANNOVAR software on GitHub

- Summary
- Related research
  (9)

tips_and_updates
Recommended

Abstract

Documentation for the ANNOVAR software

9 Research products, page 1 of 1

A loss-of-function variant in SUV39H2 identified in autism-spectrum disorder causes altered H3K9 trimethylation and dysregulation of protocadherin β-cluster genes in the developing brain
2021IsRelatedTo
Reconstructing mutational lineages in breast cancer by multi-patient-targeted single-cell DNA sequencing
2021IsRelatedTo
Recurrent pre-leukemic deletions in myeloid malignancies are the result of DNA double-strand breaks followed by microhomology-mediated end joining
2020IsRelatedTo
Genetic Findings of Sanger and Nanopore Single-Molecule Sequencing in Patients with X-Linked Hearing Loss and Incomplete Partition Type III
2021IsRelatedTo
Recurrent deletions in clonal hematopoiesis are driven by microhomology-mediated end joining
2021IsRelatedTo
Identification and Prioritisation of Variants in the Short Open-Reading Frame Regions of the Human Genome
2017IsRelatedTo
Transcriptome analysis provides critical answers to the “variants of uncertain significance” conundrum
2022IsRelatedTo
Immunohistochemical and molecular evolutionary features of jejunoileal adenocarcinoma unveiled through comparative analysis with colorectal adenocarcinoma
2025IsRelatedTo
Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development
2022IsRelatedTo