International Publications
Publisher:
Time: 31/01/2023
This publication supports for the following genetic testing:
Publisher:
Time: 08/05/2023
This publication supports for the following genetic testing:
Publisher:
Time: 13/03/2023
This publication supports for the following genetic testing:
Được công bố tại:
Ngày đăng: 30/01/2022
Publisher:
Time: 05/01/2022
This publication supports for the following genetic testing:
Publisher
Time: 30/01/2022
This publication supports for the following genetic testing:
Publisher:
Time: 16/12/2022
This publication supports for the following genetic testing:
Key findings: Detect ctDNA in 90.5% of the pre-operative plasma samples, whereas carcinoembryonic antigen (CEA) was elevated in only 41.3% of them.
Publisher:
Time: 12/12/2022
This publication supports for the following genetic testing:
Key findings: Asian cohorts show higher TP53 mutation frequency than in Caucasians. Alterations in PIK3CA and PI3K signaling were dominant.
Publisher:
Time: 10/12/2022
This publication supports for the following genetic testing:
Key findings: Develop a personalized, tumor-informed assay to detect circulating tumor DNA (ctDNA) in liquid biopsy with high sensitivity and specificity using ultra-deep next-generation sequencing (NGS)
Publisher:
Time: 27/04/2022
This publication supports for the following genetic testing:
Key findings: Evaluate SPOT-MAS performance on detection of 4 common cancer types
Publisher:
Time: 27/04/2022
This publication supports for the following genetic testing:
Key finding:
Publisher:
Time: 22/02/2021
This publication supports for the following genetic testing:
Key finding:
Publisher:
Time: 12/08/2021
This publication supports for the following genetic testing:
Key finding:
Publisher:
Time: 04/08/2020
This publication supports for the following genetic testing:
Key finding: Identify cancer actionable mutations of NSCLC using plasma cfDNA
Publisher:
Time: 17/02/2020
This publication supports for the following genetic testing:
The identification and quantification of actionable mutations are of critical importance for effective genotype-directed therapies, prognosis and drug response monitoring in patients with non-small-cell lung cancer (NSCLC)…
Publisher:
Time: 24/01/2020
This publication supports for the following genetic testing:
Key finding: Present a novel method to detect cancer-specific mutation in blood samples of NSCLC patients
Publisher:
Time: 16/12/2019
This publication supports for the following genetic testing:
Key findings: Identify 295 (0.279%) suspected MMXO cases. After FISH analysis, MMXO was confirmed in 125 cases (42.37%), revealing the MMXO prevalence of 0.118% (95% CI: 0.097–0.139%)
Publisher:
Time: 13/12/2022
This publication supports for the following genetic testing:
Publisher:
Time: 22/08/2022
This publication supports for the following genetic testing:
Key findings: 68,885 Vietnamese pregnant women were recruited and α-thalassemia statuses were determined by gap-PCR, revealing 5344 women (7.76%) carried deletions including αα/−−SEA (4.066%), αα/−α3.7 (2.934%), αα/−α4.2 (0.656%), and rare genotypes (0.102%)
Publisher:
Time: 09/08/2022
This publication supports for the following genetic testing:
Thiết lập được qui trình sàng lọc trước sinh không xâm lấn bằng kỹ thuật giải trình tự thế hệ mới cho nhiều bệnh đơn gen với độ chính xác cao.
Được công bố tại:
Ngày đăng: 27/04/2022
Nghiên cứu ứng dụng cho xét nghiệm:
Publisher:
Time: 07/07/2021
This publication supports for the following genetic testing:
Publisher:
Time: 05/11/2020
This publication supports for the following genetic testing:
NIPT TriSure có giá trị tiên đoán dương PPV chung cho ba loại bất thường T21, T18, T13 là 94,3% chứng minh khảnăng đáng tin cậy của xét nghiệm sàng lọc tiền sản này trong việc phát hiện các lệch bội nhiễm sắc thể phổ biến
Được công bố tại:
Ngày đăng: 01/04/2020
Nghiên cứu ứng dụng cho xét nghiệm:
Key findings: Reveal 24,487 disease-associated genetic variants and their allele frequency distribution, especially 5 pathogenic variants for prevalent genetic disorders in Vietnam
Publisher:
Time: 08/12/2019
This publication supports for the following genetic testing:
Publisher:
Time: 04/02/2019
This publication supports for the following genetic testing:
Publisher:
Time: 10/07/2018
This publication supports for the following genetic testing:
Ứng dụng kỹ thuật này với 68 mẫu máu của các thai phụ có tuần tuổi thai từ 14 tuần đến 16 tuần. Kết quả phát hiện 34 trường hợp có bất thường NST bao gồm 26 Trisomy 21, 6 Trisomy 18 và 2 Trisomy 13 và 34 mẫu bình thường. So sánh kết quả của phương pháp giải trình tự gen thế hệ mới với kết quả nhiễm sắc thể đồ tại Bệnh viện Hùng Vương cho thấy sự tương đồng giữa các phương pháp là 100%.
Được công bố tại:
Ngày đăng: Năm 2017
Nghiên cứu ứng dụng cho xét nghiệm:
Publisher:
Time: 05/2010
Publisher:
Time: 05/2010
Publisher:
Time: 26/02/2014
Publisher:
Time: 21/05/2014
Publisher:
Time: 18/06/2015
Publisher:
Time: 28/07/2015
Key finding: for the first time the use of massively parallel sequencing (MPS)-based genetic testing to identify a germline mutation within a three-generation Vietnamese family
Publisher:
Time: 19/10/2018
Key finding: the diagnosis of Joubert syndrome in a Vietnamese family and expands the mutational spectrum of TMEM67 sequence variations
Publisher:
Time: 30/01/2020
Key finding: Identify four missense mutations in APP/PSEN1 genes from six individuals, which accounts for 11.8% of all tested cases
Publisher:
Time: 21/02/2020
Key finding: Of 3259 women screened across Vietnam, 450 (13.8%) carried disease-associated variants for G6PD, PAH and GALT. The prevalence of carriers was 8.9% (291 of 3259) in G6PD and 4.6% (152 of 3259) in PKU, whilst GAL was low at 0.2% (7 of 3259). Two GALT variants, c.593 T > C and c.1034C > A, have rarely been reported.
Publisher:
Time: 03/05/2022
Key finding: Early disease diagnosis with bile acid replacement therapy for 3 clinical congenital bile acid synthesis defect cases in the Vietnamese population.
Publisher:
Time: 24/06/2022