Pengyuan Zhu

Guangzhou, China

Last Updated: 09/26/2026

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Found 12 publications

Comparative performance evaluation of FilmArray RP 2.1 and targeted next-generation sequencing in upper respiratory tract infections.

Comparative performance evaluation of FilmArray RP 2.1 and targeted next-generation sequencing in upper respiratory tract infections.

Journal: Frontiers in cellular and infection microbiology
Published: April 12, 2025

Diagnosis value of targeted and metagenomic sequencing in respiratory tract infection.

Diagnosis value of targeted and metagenomic sequencing in respiratory tract infection.

Journal: Frontiers in cellular and infection microbiology
Published: September 19, 2024

Enhancing lower respiratory tract infection diagnosis: implementation and clinical assessment of multiplex PCR-based and hybrid capture-based targeted next-generation sequencing.

Enhancing lower respiratory tract infection diagnosis: implementation and clinical assessment of multiplex PCR-based and hybrid capture-based targeted next-generation sequencing.

Journal: EBioMedicine
Published: April 13, 2024

Different Circulation Pattern of Multiple Respiratory Viruses in Southern China During the COVID-19 Pandemic.

Different Circulation Pattern of Multiple Respiratory Viruses in Southern China During the COVID-19 Pandemic.

Journal: Frontiers in microbiology
Published: October 26, 2021

A targeted gene capture next-generation sequencing panel for genetic screening of newborns.

A targeted gene capture next-generation sequencing panel for genetic screening of newborns.

Journal: JPMA. The Journal of the Pakistan Medical Association
Published: November 07, 2020

Genetic screening involving 101 hot spots for neonates not passing newborn hearing screening and those random recruited in Dongguan.

Genetic screening involving 101 hot spots for neonates not passing newborn hearing screening and those random recruited in Dongguan.

Journal: International journal of pediatric otorhinolaryngology
Published: May 08, 2018

A novel mutation in the SLC26A4 gene in a Chinese family with non-syndromic hearing loss and enlarged vestibular aqueduct.

A novel mutation in the SLC26A4 gene in a Chinese family with non-syndromic hearing loss and enlarged vestibular aqueduct.

Journal: International journal of pediatric otorhinolaryngology
Published: August 24, 2017

A novel variant in the CDH23 gene is associated with non-syndromic hearing loss in a Chinese family.

A novel variant in the CDH23 gene is associated with non-syndromic hearing loss in a Chinese family.

Journal: International journal of pediatric otorhinolaryngology
Published: August 15, 2017

A novel mutation in the MYO7A gene is associated with Usher syndrome type 1 in a Chinese family.

A novel mutation in the MYO7A gene is associated with Usher syndrome type 1 in a Chinese family.

Journal: International journal of pediatric otorhinolaryngology
Published: March 13, 2017

A novel missense mutation in the SLC26A4 gene causes nonsyndromic hearing loss and enlarged vestibular aqueduct.

A novel missense mutation in the SLC26A4 gene causes nonsyndromic hearing loss and enlarged vestibular aqueduct.

Journal: International journal of pediatric otorhinolaryngology
Published: November 03, 2016

Correction: OTG-snpcaller: An Optimized Pipeline Based on TMAP and GATK for SNP Calling from Ion Torrent Data.

Correction: OTG-snpcaller: An Optimized Pipeline Based on TMAP and GATK for SNP Calling from Ion Torrent Data.

Journal: PloS one
Published: September 17, 2015

OTG-snpcaller: an optimized pipeline based on TMAP and GATK for SNP calling from ion torrent data.

OTG-snpcaller: an optimized pipeline based on TMAP and GATK for SNP calling from ion torrent data.

Journal: PloS one
Published: December 04, 2013
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Last Updated: 09/26/2026