Clinical next generation sequencing trang 1 tải miễn phí từ TAILIEUCHUNG

"Clinical next generation sequencing" trang 1 - tải miễn phí từ Tailieuchung

Scenario drafting for early technology assessment of next generation sequencing in clinical oncology

Scenario drafting for early technology assessment of next generation sequencing in clinical oncology

10 41 1

Detailed evaluation of cancer sequencing pipelines in different microenvironments and heterogeneity levels

Detailed evaluation of cancer sequencing pipelines in different microenvironments and heterogeneity levels

13 45 1

MendeLIMS: A web-based laboratory information management system for clinical genome sequencing

MendeLIMS: A web-based laboratory information management system for clinical genome sequencing

8 27 1

Clinical phenotype-based gene prioritization: An initial study using semantic similarity and the human phenotype ontology

Clinical phenotype-based gene prioritization: An initial study using semantic similarity and the human phenotype ontology

11 56 1

Patients harboring uncommon EGFR exon 19 deletion-insertion mutations respond well to first-generation EGFR inhibitors and osimeritinib upon acquisition of T790M

Patients harboring uncommon EGFR exon 19 deletion-insertion mutations respond well to first-generation EGFR inhibitors and osimeritinib upon acquisition of T790M

9 42 1

ClinQC: A tool for quality control and cleaning of Sanger and NGS data in clinical research

ClinQC: A tool for quality control and cleaning of Sanger and NGS data in clinical research

9 26 1

GAVIN: Gene-Aware Variant INterpretation for medical sequencing

GAVIN: Gene-Aware Variant INterpretation for medical sequencing

10 44 3

Genetic and clinical characteristics of Chinese children with Glucokinasematurity-onset diabetes of the young (GCKMODY)

Genetic and clinical characteristics of Chinese children with Glucokinasematurity-onset diabetes of the young (GCKMODY)

8 81 0

Clinical application of genomic profiling to find druggable targets for adolescent and young adult (AYA) cancer patients with metastasis

Clinical application of genomic profiling to find druggable targets for adolescent and young adult (AYA) cancer patients with metastasis

10 46 1

Clinical mutational profiling and categorization of BRAF mutations in melanomas using next generation sequencing

Clinical mutational profiling and categorization of BRAF mutations in melanomas using next generation sequencing

10 70 0

DETECT I & DETECT II: A study protocol for a prospective multicentre observational study to validate the UroMark assay for the detection of bladder cancer from urinary cells

DETECT I & DETECT II: A study protocol for a prospective multicentre observational study to validate the UroMark assay for the detection of bladder cancer from urinary cells

7 76 1

Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria

Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria

11 24 1

Rapid and precise alignment of raw reads against redundant databases with KMA

Rapid and precise alignment of raw reads against redundant databases with KMA

8 30 1

Launching genomics into the cloud: Deployment of Mercury, a next generation sequence analysis pipeline

Launching genomics into the cloud: Deployment of Mercury, a next generation sequence analysis pipeline

11 43 1

The emerging clinical relevance of genomic profiling in neuroendocrine tumours

The emerging clinical relevance of genomic profiling in neuroendocrine tumours

7 19 1

Cancer of unknown primary with EGFR mutation successfully treated with targeted therapy directed by clinical next-generation sequencing: A case report

Cancer of unknown primary with EGFR mutation successfully treated with targeted therapy directed by clinical next-generation sequencing: A case report

5 32 1

A burden of rare variants in BMPR2 and KCNK3 contributes to a risk of familial pulmonary arterial hypertension

A burden of rare variants in BMPR2 and KCNK3 contributes to a risk of familial pulmonary arterial hypertension

8 16 1

Expanding the potential genes of inborn errors of immunity through protein interactions

Expanding the potential genes of inborn errors of immunity through protein interactions

8 8 1

Association of emergence of new mutations in circulating tumuor DNA during chemotherapy with clinical outcome in metastatic colorectal cancer

Association of emergence of new mutations in circulating tumuor DNA during chemotherapy with clinical outcome in metastatic colorectal cancer

10 47 1

Clinical value of next generation sequencing of plasma cell-free DNA in gastrointestinal stromal tumors

Clinical value of next generation sequencing of plasma cell-free DNA in gastrointestinal stromal tumors

12 65 1

Đã phát hiện trình chặn quảng cáo AdBlock

Trang web này phụ thuộc vào doanh thu từ số lần hiển thị quảng cáo để tồn tại. Vui lòng tắt trình chặn quảng cáo của bạn hoặc tạm dừng tính năng chặn quảng cáo cho trang web này.