Genomics News and Research

RSS
ESMO: New system to rank relevance of treatable cancer genetic mutations needed

ESMO: New system to rank relevance of treatable cancer genetic mutations needed

Research identifies link between rare gene variants and survival after blood and marrow transplant

Research identifies link between rare gene variants and survival after blood and marrow transplant

New system promises greater accuracy in determining heart transplant rejection and injury

New system promises greater accuracy in determining heart transplant rejection and injury

Scientists develop indices that provide information about prognosis of cancers

Scientists develop indices that provide information about prognosis of cancers

Insilico to present recent advances in AI for aging biomarkers and age management research

Insilico to present recent advances in AI for aging biomarkers and age management research

Human genome is like a time machine, says researcher

Human genome is like a time machine, says researcher

Computational biologists develop algorithm to align datasets with single-cell resolution

Computational biologists develop algorithm to align datasets with single-cell resolution

FDA-approved inhibitors could be repurposed to target ARID1A-mutant ovarian cancers

FDA-approved inhibitors could be repurposed to target ARID1A-mutant ovarian cancers

Researchers probe RNA epigenetics and chromatin structures to predict drug resistance in leukemia

Researchers probe RNA epigenetics and chromatin structures to predict drug resistance in leukemia

Genetic mutation that may protect people from malaria found to be more common

Genetic mutation that may protect people from malaria found to be more common

New computational method helps to identify tumor cell mutations with greater accuracy

New computational method helps to identify tumor cell mutations with greater accuracy

Genomics England announces appointment of global genomics pioneer as first CEO

Genomics England announces appointment of global genomics pioneer as first CEO

Groundbreaking 100,000 Genomes Project achieves important milestone to transform NHS care

Groundbreaking 100,000 Genomes Project achieves important milestone to transform NHS care

Wales participates in the 100,000 Genomes Project

Wales participates in the 100,000 Genomes Project

Verge joins Genomics England’s Discovery Forum industry partnership

Verge joins Genomics England’s Discovery Forum industry partnership

Genomics England announces new partnership to improve efficiency of next-generation sequencing analysis

Genomics England announces new partnership to improve efficiency of next-generation sequencing analysis

Scotland study aims to offer precise diagnoses for people with rare genetic diseases

Scotland study aims to offer precise diagnoses for people with rare genetic diseases

Whole Genome Sequencing used as diagnostic solution for TB

Whole Genome Sequencing used as diagnostic solution for TB

Researchers develop way to sequence entire fetal genome by modifying prenatal testing method

Researchers develop way to sequence entire fetal genome by modifying prenatal testing method

Researchers identify novel gene involved in familial breast cancer

Researchers identify novel gene involved in familial breast cancer

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.