Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Topics Community

Article

Unraveling epigenomic abnormality in azoospermic human males by WGBS, RNA-Seq, and transcriptome profiling analyses

13 Feb 2020

Abstract excerpt

No abstract is available from the source.

Topics

Join the communities discussing this publication.

Epigenetics and DNA Methylation
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Sperm and Testicular Function

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 32056059
DOI: 10.1007/s10815-020-01716-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Unraveling epigenomic abnormality in azoospermic human males by WGBS, RNA-Seq, and transcriptome profiling analysesPMID 32056059Read ↗

Evaluating genetic causes of azoospermia: What can we learn from a complex cellular structure and single-cell transcriptomics of the human testis?Semantic proximity Read ↗

Genetic Architecture of Azoospermia—Time to Advance the Standard of CareSemantic proximity Read ↗

Decoding dynamic epigenetic landscapes in human oocytes using single-cell multi-omics sequencingSemantic proximity Read ↗

Summarizing the human genes and their variants causative of non-obstructive azoospermia uncovered using whole genome/exome sequencingSemantic proximity Read ↗

Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermiaSemantic proximity Read ↗

Genetic and epigenetic insights into non-obstructive azoospermia: mechanisms, biomarkers, and clinical perspectivesSemantic proximity Read ↗

Single-cell sequencing in non-obstructive azoospermia: insights from primary and re-analysis studiesSemantic proximity Read ↗

Genome wide abnormal DNA methylome of human blastocyst in assisted reproductive technologySemantic proximity Read ↗

Human spermatogonial stem cells and their niche in male (in)fertility: novel concepts from single-cell RNA-sequencingSemantic proximity Read ↗

Genetic and epigenetic profiling of the infertile maleSemantic proximity Read ↗

Human zygotic genome activation is initiated from paternal genomeSemantic proximity Read ↗

A multi-omics genome-and-transcriptome single-cell atlas of human preimplantation embryogenesis reveals the cellular and molecular impact of chromosome instabilitySemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.