Whole Genome Sequencing News and Research

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Insights into the products and services of Azenta

Insights into the products and services of Azenta

Early-life acquisition of antibiotic resistance in neonates from developing countries

Early-life acquisition of antibiotic resistance in neonates from developing countries

Children with intellectual disability of genetic origin are extremely likely to develop other neuropsychiatric conditions

Children with intellectual disability of genetic origin are extremely likely to develop other neuropsychiatric conditions

What is the prevalence of carbapenem-resistant Enterobacterales among individuals with and without health risk factors?

What is the prevalence of carbapenem-resistant Enterobacterales among individuals with and without health risk factors?

Study assesses eight de novo genome assembly software tools on viral next-generation sequencing data

Study assesses eight de novo genome assembly software tools on viral next-generation sequencing data

Novel blood test offers unprecedented insight into a patient's cancer make-up

Novel blood test offers unprecedented insight into a patient's cancer make-up

Scientists provide first report from the largest whole genome sequencing effort to date

Scientists provide first report from the largest whole genome sequencing effort to date

Study shows Omicron BA.4/5 infection triggers highly cross-reactive neutralizing antibodies

Study shows Omicron BA.4/5 infection triggers highly cross-reactive neutralizing antibodies

WHO issues an urgent call to accelerate access to genomics in resource-poor countries

WHO issues an urgent call to accelerate access to genomics in resource-poor countries

MINAR2 gene mutations cause progressive hearing loss

MINAR2 gene mutations cause progressive hearing loss

Study illustrates how the use of whole exome sequencing can better predict treatment response

Study illustrates how the use of whole exome sequencing can better predict treatment response

Roundworms shed light on vision loss in a rare human genetic disorder

Roundworms shed light on vision loss in a rare human genetic disorder

Rapid test can identify which variant has infected a COVID-19 patient in just a few hours

Rapid test can identify which variant has infected a COVID-19 patient in just a few hours

Inherited mutations in the MINAR2 gene lead to sensorineural deafness

Inherited mutations in the MINAR2 gene lead to sensorineural deafness

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

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

Researchers show the feasibility of a comprehensive sequencing approach in pediatric and young adult cancers

Researchers show the feasibility of a comprehensive sequencing approach in pediatric and young adult cancers

PerkinElmer expands genomic testing services with ultrarapid whole genome sequencing

PerkinElmer expands genomic testing services with ultrarapid whole genome sequencing

seqWell’s plexWell technology selected by California Conservation Genomics Project for conservation genomics research

seqWell’s plexWell technology selected by California Conservation Genomics Project for conservation genomics research

Insight into Neurological Diagnosis in Children

Insight into Neurological Diagnosis in Children

Evaluating the findings of phase 3 clinical trial of plant-based COVID-19 vaccine

Evaluating the findings of phase 3 clinical trial of plant-based COVID-19 vaccine