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In a groundbreaking study poised to reshape the landscape of pancreatic cancer research, Chen, Lou, Guo, and colleagues have unveiled a sophisticated approach that links genetic mu...
New chromatin‑based analysis of 1,563 AML samples reveals 16 epigenomic subgroups that improve prognostic accuracy and highlight unexpected drug sensitivities. The post Epigenomic...
Acute lymphoblastic leukemia (ALL), a malignancy of the lymphoid progenitor cells, has long been a focus of intense biomedical research due to its aggressive nature and prevalence...
Despite remarkable progress in medical science, the prognosis for most patients diagnosed with advanced-stage cancers remains bleak. The challenge lies not only in the complexity o...
A groundbreaking study has unveiled a novel proteomic landscape underlying SMARCA-deficient esophageal adenocarcinoma (EAC), shedding light on new mechanisms of tumor progression a...
“Guardian of the genome,” p53 is now therapeutically accessible using CRISPR-based technology from Jennifer Doudna’s lab. The approach uses RNA signatures to identify and destroy t...
Ahead of ASCO 2026, Illumina unveiled an early-access MRD research kit using whole-genome sequencing and DRAGEN analysis, enabling highly sensitive cancer monitoring workflows on N...
Officials said the new facility is expected to enhance access to modern cancer care and improve treatment outcomes for patients in Telangana and neighbouring states
Thousands of cancer patients have untapped treatment options in their genomic data. Now they can find them. Available in 12 states, expanding nationwide.
In the rapidly evolving landscape of cancer research, the three-dimensional structure of the genome has emerged as a critical frontier. Recent studies have unveiled how the spatial...
Developing software to reveal large genetic changes that lead to cancer
In recent years, the concept of “junk DNA” has undergone a dramatic transformation in the field of cancer biology, shifting from perceived biological detritus to a treasure trove o...
RNA sequencing reveals distinct cellular programs and therapeutic targets in rare sinonasal carcinomas, supporting precision oncology approaches tailored to specific tumor subtypes...
Source: National University of Singapore From: news-medical.net A study led by Dr Jason Pitt, Principal Investigator at the Cancer Science Institute of Singapore (CSI Singapore), h...
RNA sequencing and nanopore sequencing enabled Eclipse-like full transcriptome analysis to identify novel non-coding RNA biomarkers in extracellular vesicles for early esophageal.....
[Institut Pasteur de Dakar] First 40 human whole genomes sequenced using Illumina and Oxford Nanopore Technologies platforms Institut Pasteur de Dakar launches clinical laboratory...
A human‑in‑the‑loop AI framework rapidly nominates CAR T targets, leading to a GPNMB‑directed CAR T cell with activity across melanoma, leukemia, and colorectal cancer in preclinic...
In a groundbreaking advance that promises to reshape our understanding of breast cancer, a team of international researchers has harnessed the power of multi-ancestry transcriptome...
For decades, the scientific community has recognized the gut microbiome—the intricate ecosystem of bacteria and microorganisms residing within the human intestine—as a potential ke...
Did you know that one in 10 Americans have a rare disease and it can take five or more years, on average, for a person with a rare disease to get an accurate diagnosis? That’s more...
Researchers at McGill University have made a groundbreaking discovery that sheds light on the genetic factors contributing to the heightened risk of pancreatic cancer observed in s...
A collaborative study used whole-genome sequencing to examine the genetic makeup of 110 children from Aosta Valley (Valle d'Aosta) with neurodevelopmental disorders and their paren...
RNA sequencing enabled comprehensive detection of clinically relevant gene fusions in acute leukemia, including rare rearrangements that conventional diagnostic methods failed to i...
The goal of the partnership is to build a precision medicine hub for cancer patients around the globe using MSK’s clinical data and Sophia Genetics’ AI platform.
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