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Jingqing Hu

dblp:146/4109 · DBLP profile ↗
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3ranked-venue papers
1as first author
1since 2021 · last 2026
0009-0008-2880-9940ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 3 · 1 first-author · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › immunoinformatics
HLA typing
1.012026
FuFiHLA: a tool for full-field HLA typing from long-read data · Bioinform. 2026
Bioinformatics and computational biology › sequence analysis › sequence assembly
consensus sequence generation
0.312026
FuFiHLA: a tool for full-field HLA typing from long-read data · Bioinform. 2026
Bioinformatics and computational biology › genomics › next-generation sequencing data analysis
long-read sequencing analysis
0.312026
FuFiHLA: a tool for full-field HLA typing from long-read data · Bioinform. 2026

Methods — techniques the papers use, named apart from their topics

long-read alignment · 1.0consensus calling · 1.0
YearPublicationVenuePosition
2026 FuFiHLA: a tool for full-field HLA typing from long-read data
abstract
MOTIVATION: Allele typing for Human Leukocyte Antigen (HLA) genes has many important clinical applications. Popular short-read typing can only accurately distinguish alleles at the coding sequence level, which potentially limit our understanding of the effect of variants in non-coding region. Long read data has been proved to be useful in typing HLA alleles in full resolution, but only a few tools are publicly available and with significant limitations in practical application. RESULTS: We developed FuFiHLA, a lightweight open-source software, to type HLA alleles. Currently it supports typing alleles of six HLA genes (HLA-A, HLA-B, HLA-C, HLA-DRB1, HLA-DQA1, and HLA-DQB1) from long reads. Evaluation using 233 PacBio HiFi WGS samples from HPRC shows that FuFiHLA achieves 99.6% accuracy in the full field allele typing and QV as 51.8 for consensus allele sequence construction. Additional testing on four Nanopore R10 reads demonstrates slightly reduced accuracy in the fourth field. AVAILABILITY: FuFiHLA is available at https://github.com/jingqing-hu/FuFiHLA under MIT License.
Jingqing Hu
Bioinform.1
2013 Integrating phenotype-genotype data for prioritization of candidate symptom genes
abstract
Symptoms and signs (symptoms in brief) are the essential clinical manifestations for traditional Chinese medicine (TCM) diagnosis and treatments. To gain insights into the molecular mechanism of symptoms, this paper presents a network-based data mining method to integrate multiple phenotype-genotype data sources and predict the prioritizing gene rank list of symptoms. The result of this pilot study suggested some insights on the molecular mechanism of symptoms.
Xuezhong Zhou, Yonghong Peng, Runshun Zhang, Jingqing Hu, Jian Yu 0001, Baoyan Liu
BIBM5
2013 Complex network approach for analyzing TCM clinical herb-symptom relationships
abstract
Traditional Chinese Medicine (TCM) is a discipline of clinical medicine, which focuses on individualized diagnosis and treatment based on observation of the clinical manifestations of real-world patients. The complicated interactions between different medical entities play significant role for individualized treatment. In this paper, we aim to find out the meaningful herb-symptom relationship from large number of clinical data with using complex network approach. We construct two different patient networks to verify the positive correlations between herbs and symptoms in TCM clinical treatment.
Xuezhong Zhou, Runshun Zhang, Jingqing Hu, Qi Xie 0005, Baoyan Liu
BIBM5