Machine-learning immune-system analysis study may hold clues to personalized medicine

How people with compromised immune systems respond to vaccines is an important area of immunological research. A study led by ...

FamilyTreeDNA Advances Genetic Genealogy with Precision Genomics Partnership

The panel ensures compatibility with our previous autosomal Family Finder tests plus all the autosomal transfers we ...
Journal of Medical Genetics

Inherited variants in autosomal dominant disease genes are a significant cause of fetal structural anomalies

Background Monogenic disorders are a major cause of fetal structural anomalies. Most genetic diagnoses involve de novo, biallelic or X linked variants; however, inherited variants in autosomal ...
Frontiers

Correction: Identification and analysis of diverse cell death patterns in osteomyelitis via microarray-based transcriptome profiling and clinical data

An incorrect Funding statement was provided. The correct Funding statement reads: “The author(s) declare that financial support was received for the research and/or publication of this article. This ...
Frontiers

Identification and analysis of diverse cell death patterns in osteomyelitis via microarray-based transcriptome profiling and clinical data

Osteomyelitis (OM) is a debilitating infectious disease characterized by inflammation of the bone and bone marrow. Emerging evidence suggests that multiple forms of programmed cell death (PCD) ...
BioSpace

Bionano Announces Upgrades to its Software and Compute Platforms to Make Analysis of OGM, Microarray and NGS Data Easier, Faster and More Accurate

SAN DIEGO, Aug. 05, 2025 (GLOBE NEWSWIRE) -- Bionano Genomics, Inc. (NASDAQ: BNGO) today announced the release of the latest versions of its VIA™ and Solve™ software for genomic data analysis and ...
IEEE

A software pipeline for multiple microarray data analysis

Abstract: Microarray platforms such as Gene expression, oligonucleotide (GeneChip), and cDNA (complementary DNA) can play a critical role in the understanding of genome sequencing, by providing ...
EurekAlert!

GenEditScan: novel k-mer analysis tool based on next-generation sequencing for foreign DNA detection in genome-edited products

The presence or absence of remaining foreign DNA from the crossbred progeny of the genome-edited crop and the original crop cultivar can be determined by GenEditScan, based on the k-mer method.
GitHub

Investigating the performance of Oxford Nanopore long-read sequencing with respect to Illumina microarrays and short-read sequencing

This repository contains the complete workflow and analysis scripts for benchmarking Oxford Nanopore Technologies (ONT) long-read sequencing against established platforms (Illumina short-read ...