Genomics

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Whole-genome sequencing can help provide an accurate diagnosis of severely ill infants

Children who are born severely ill or who develop serious illness in the first few weeks of life are often difficult to diagnose, with considerable implications for their short and longer-term care.

13 Jun 2022

New machine learning algorithm finds a gene signature characteristic of tumors

How do cancer cells differ from healthy cells? A new machine learning algorithm called "ikarus" knows the answer, reports a team led by MDC bioinformatician Altuna Akalin in the journal Genome Biology. The AI program has found a gene signature characteristic of tumors.

10 Jun 2022

Proteomic analysis of 2002 tumors reveals 11 distinct pan-cancer molecular subtypes

A new study that analyzed protein levels in 2,002 primary tumors from 14 tissue-based cancer types identified 11 distinct molecular subtypes, providing systematic knowledge that greatly expands a searchable online database that has become a go-to platform for cancer data analysis by users worldwide.

10 Jun 2022

Genomic analysis provides a deeper understanding of DCIS biology

A new study led by the global Cancer Grand Challenges PRECISION team, including researchers from The University of Texas MD Anderson Cancer Center, shifts the long-held belief that all invasive breast cancers following ductal carcinoma in situ (DCIS) arise from the original DCIS lesion.

9 Jun 2022

Infiltrating gliomas are shaped by genetic evolution and microenvironment, finds study

Researchers have discovered that infiltrating gliomas, a common brain and spinal cord tumor, are shaped by their genetic evolution and microenvironment, a finding that could lead to more targeted treatments.

9 Jun 2022

Researchers create first comprehensive functional map of genes expressed in human cells

The Human Genome Project was an ambitious initiative to sequence every piece of human DNA. The project drew together collaborators from research institutions around the world, including Whitehead Institute, and was finally completed in 2003.

9 Jun 2022

Curia and Replicate Bioscience Enter Strategic Collaboration to Create Groundbreaking Development Platform for Self-Replicating RNA (srRNA)

From Curia 9 Jun 2022

Stem cell models help determine previously unknown genetic markers of glaucoma

Stem cell models of the retina and optical nerve have been used to identify previously unknown genetic markers of glaucoma, in research jointly led by scientists from the Garvan Institute of Medical Research, the University of Melbourne, and the Centre for Eye Research Australia.

9 Jun 2022

Most synonymous genetic mutations are strongly harmful, study shows

In the early 1960s, University of Michigan alumnus Marshall Nirenberg and a few other scientists deciphered the genetic code of life, determining the rules by which information in DNA molecules is translated into proteins, the working parts of living cells.

8 Jun 2022

Genomics

Whole-genome sequencing can help provide an accurate diagnosis of severely ill infants

New machine learning algorithm finds a gene signature characteristic of tumors

Proteomic analysis of 2002 tumors reveals 11 distinct pan-cancer molecular subtypes

Genomic analysis provides a deeper understanding of DCIS biology

Infiltrating gliomas are shaped by genetic evolution and microenvironment, finds study

Researchers create first comprehensive functional map of genes expressed in human cells

Curia and Replicate Bioscience Enter Strategic Collaboration to Create Groundbreaking Development Platform for Self-Replicating RNA (srRNA)

Stem cell models help determine previously unknown genetic markers of glaucoma

Most synonymous genetic mutations are strongly harmful, study shows

Detailed genetic roadmap of glaucoma will help develop new drugs to combat the disease

How do viruses evolve to infect new hosts?

Study reveals how common drug-resistant superbug responds to ‘last resort’ antibiotic

Study offers insights into genetic factors that affect immunological responses in type 1 diabetes

Study finds striking epigenetic differences in the airway cells of adult children born to asthmatic mothers

Study offers recommendations for improving statistical inference in population genomics

Addressing the ‘trust factor’: South Carolina researchers tackle health disparities using genetics

Combinations of multiple genetic factors play a role in the broad spectrum of autism

Steady-state DNA motion allows cells to conduct housekeeping tasks under similar nuclear environments

Lack of diversity in genomic research could deprive Africans of life-changing care for chronic diseases

Study offers clues about the shift of harmless environmental bacterium to a dreaded pathogen

Small solutions for big problems in drug discovery and delivery

Professor Nancy Ip: Pioneering New Paths in Neurodegenerative Therapy

Utilizing process Raman in optimizing cultivated meat production

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