Evidence map›Paper›PMID 41720969›Full record

ArticleCommunications medicine2026

The clinical utility of genome sequencing is multi-dimensional: experience from the Hong Kong Genome Project.

Annie Tsz Wai Chu, Claudia Ching Yan Chung, Ho Ming Luk, Shirley Sze Wing Cheng, Robin Hayeems, Stephanie Luca, Brian Hon Yin Chung

Abstract read
In one paragraph

Article in Communications medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Annie Tsz Wai Chu *Hong Kong Genome Institute, Hong Kong Special Administrative Region, Hong Kong, China.
Claudia Ching Yan Chung *Hong Kong Genome Institute, Hong Kong Special Administrative Region, Hong Kong, China.
Ho Ming LukDepartment of Clinical Genetics, Hong Kong Children's Hospital, Hong Kong Special Administrative Region, Hong Kong, China.
Shirley Sze Wing ChengDepartment of Clinical Genetics, Hong Kong Children's Hospital, Hong Kong Special Administrative Region, Hong Kong, China.ORCID http://orcid.org/0000-0002-9923-7424
Robin HayeemsChild Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.
Stephanie LucaChild Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.
Brian Hon Yin ChungHong Kong Genome Institute, Hong Kong Special Administrative Region, Hong Kong, China. bhychung@genomics.org.hk.ORCID http://orcid.org/0000-0002-7044-5916

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAssessing clinical utility of genome sequencing (GS) is essential for healthcare decisions. This study quantified the multidimensional utility of GS using the validated Clinician-reported Genetic testing Utility InDEx (C-GUIDE) within a diverse rare disease cohort at the Hong Kong Genome Project.

methodsAdult and paediatric patients suspected of genetic disorders were recruited from the Hong Kong Children's Hospital. Clinical geneticists evaluated GS utility based on 17 items. Total C-GUIDE utility scores and global item scores were calculated, with individual item scores ranging from -2 to 2.

resultsBetween March and July 2024, three clinical geneticists completed 247 C-GUIDE ratings for 245 probands, with 25% receiving positive, 7% inconclusive, and 69% negative GS results. Total C-GUIDE scores ranges from -1 to 30, with a mean of 6.1 (SD = 10.0). Multivariate regression analysis indicates that positive GS findings are associated with a 16.9-point increase in C-GUIDE scores compared to inconclusive or negative results (p < 0.001). Notably, the highest mean scores are observed in psychosocial benefits for patients and families, regardless of GS results. The mean global item score, representing overall assessment of clinical utility, is 0.53 (SD = 0.06). Baseline patient characteristics are not independently associated with C-GUIDE scores.

conclusionsThis study represents the first and largest of its kind in the Asia Pacific region, highlighting the multidimensional benefits of GS and the importance of nationwide Genome Projects. By highlighting that clinical utility is primarily influenced by test results rather than patient characteristics, this study underscores the importance of equitable GS implementation across populations.

Identifiers

PMID41720969
PMCPMC13036034

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.