Xiaoming Wei

Wuhan, 430074, China

Last Updated: 09/26/2026

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Found 31 publications

RGB-T Tracking With Template-Bridged Search Interaction and Target-Preserved Template Updating.

RGB-T Tracking With Template-Bridged Search Interaction and Target-Preserved Template Updating.

Journal: IEEE transactions on pattern analysis and machine intelligence

Published: October 07, 2024

Accuracy and depth evaluation of clinical low pass genome sequencing in the detection of mosaic aneuploidies and CNVs.

Accuracy and depth evaluation of clinical low pass genome sequencing in the detection of mosaic aneuploidies and CNVs.

Journal: BMC medical genomics

Published: June 26, 2023

Validation and depth evaluation of low-pass genome sequencing in prenatal diagnosis using 387 amniotic fluid samples.

Validation and depth evaluation of low-pass genome sequencing in prenatal diagnosis using 387 amniotic fluid samples.

Journal: Journal of medical genetics

Published: December 12, 2022

A consensus on prenatal diagnosis and genetic counseling for chromosomal mosaicism

A consensus on prenatal diagnosis and genetic counseling for chromosomal mosaicism

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: August 05, 2022

Clinical diagnosis of genetic disorders at both single-nucleotide and chromosomal levels based on BGISEQ-500 platform.

Clinical diagnosis of genetic disorders at both single-nucleotide and chromosomal levels based on BGISEQ-500 platform.

Journal: Human genome variation

Published: April 26, 2022

AutoCNV: a semiautomatic CNV interpretation system based on the 2019 ACMG/ClinGen Technical Standards for CNVs.

AutoCNV: a semiautomatic CNV interpretation system based on the 2019 ACMG/ClinGen Technical Standards for CNVs.

Journal: BMC genomics

Published: April 27, 2021

The pathogenicity of novel GUCY2D mutations in Leber congenital amaurosis 1 assessed by HPLC-MS/MS.

The pathogenicity of novel GUCY2D mutations in Leber congenital amaurosis 1 assessed by HPLC-MS/MS.

Journal: PloS one

Published: November 11, 2019

An APC Mutation in a Large Chinese Kindred With Familial Adenomatous Polyposis Was Identified Using Both Next Generation Sequencing and Simple STR Marker Haplotypes.

An APC Mutation in a Large Chinese Kindred With Familial Adenomatous Polyposis Was Identified Using Both Next Generation Sequencing and Simple STR Marker Haplotypes.

Journal: Frontiers in genetics

Published: July 19, 2019

Sub-Exome Target Sequencing in a Family With Syndactyly Type IV Due to a Novel Partial Duplication of the LMBR1 Gene: First Case Report in Fujian Province of China.

Sub-Exome Target Sequencing in a Family With Syndactyly Type IV Due to a Novel Partial Duplication of the LMBR1 Gene: First Case Report in Fujian Province of China.

Journal: Frontiers in genetics

Published: December 04, 2018

Targeted next-generation sequencing as a comprehensive test for Mendelian diseases: a cohort diagnostic study.

Targeted next-generation sequencing as a comprehensive test for Mendelian diseases: a cohort diagnostic study.

Journal: Scientific reports

Published: March 12, 2018

Application of an improved targeted next generation sequencing method to diagnose non‑syndromic mental retardation in one step: A case report.

Application of an improved targeted next generation sequencing method to diagnose non‑syndromic mental retardation in one step: A case report.

Journal: Molecular medicine reports

Published: October 18, 2017

Identification of a Disease-Causing Mutation in a Chinese Patient with Retinitis Pigmentosa by Targeted Next-Generation Sequencing.

Identification of a Disease-Causing Mutation in a Chinese Patient with Retinitis Pigmentosa by Targeted Next-Generation Sequencing.

Journal: European journal of ophthalmology

Published: April 22, 2017

Showing 1-12 of 31

Last Updated: 09/26/2026