[HTML] nih.gov

[HTML][HTML] Long-read genome sequencing and variant reanalysis increase diagnostic yield in neurodevelopmental disorders

SM Hiatt, JMJ Lawlor, LH Handley, DR Latner… - medRxiv - ncbi.nlm.nih.gov
Variant detection from long-read genome sequencing (lrGS) has proven to be considerably
more accurate and comprehensive than variant detection from short-read genome …
相关文章

Long-read genome sequencing and variant reanalysis increase diagnostic yield in neurodevelopmental disorders

SM Hiatt, JMJ Lawlor, LH Handley, DR Latner… - medRxiv, 2024 - medrxiv.org
Variant detection from long-read genome sequencing (lrGS) has proven to be considerably
more accurate and comprehensive than variant detection from short-read genome …

Long-read genome sequencing and variant reanalysis increase diagnostic yield in neurodevelopmental disorders

SM Hiatt, JMJ Lawlor, LH Handley… - … : the preprint server …, 2024 - pubmed.ncbi.nlm.nih.gov
Variant detection from long-read genome sequencing (lrGS) has proven to be considerably
more accurate and comprehensive than variant detection from short-read genome …

Long-read genome sequencing and variant reanalysis increase diagnostic yield in neurodevelopmental disorders.

SM Hiatt, JMJ Lawlor, LH Handley… - Medrxiv: the Preprint …, 2024 - europepmc.org
Variant detection from long-read genome sequencing (lrGS) has proven to be considerably
more accurate and comprehensive than variant detection from short-read genome …

Long-read genome sequencing and variant reanalysis increase diagnostic yield in neurodevelopmental disorders.

SM Hiatt, JM Lawlor, LH Handley… - Medrxiv: the Preprint …, 2024 - europepmc.org
Variant detection from long-read genome sequencing (lrGS) has proven to be considerably
more accurate and comprehensive than variant detection from short-read genome …