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Keyword [capture sequencing]
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1. Identification Of High-risk Human Papillomavirus Integration Sites And The Potential Mechanism Research
2. Whole Exome Capture Sequencing Identifies Candidate Genes Related To HCC
3. Preliminary Study Of Epstein-Barr Virus Strain And Integration Mechanism Based On The Whole Genome Sequencing And Virus Capture Sequencing Technology
4. The Identification Of Gene Mutation Profiling In Primary Liver Cancer And The Analysis Of Expression Pattern Of Differentiation-related Genes
5. Clinical Characteristics And Related Genes Of Heart Failure With Normal Ejection Fraction
6. Whole Exome Capture Sequencing Identifies Candidate Genes Related To Colon Cancer
7. Molecular Diagnosis In Three Inherited Retinal Disease Families Using Target Region Capture And High Through-put Sequencing
8. Accurate Detection For Hemoglobin Variants Of Thalassemia Based On Next Generation Sequencing Target Capture Technology
9. The Application Of 189-Target Capture Chip In Hereditary Retinal Diseases
10. The Screening Of Pathological Gene And The Biological Function Research Of KIT Gene In Colorectal Cancer
11. Study Of High-throughput Testing Technology And Causative Mutations For The Non-syndromic Deafness
12. Whole Exome Capture Sequencing Identifies Candidate Genes Related To Colon Liver Metastasis
13. Genetic Sequencing And Analysis Of The Mutation In A Chinese Family With Congenital Aniridia
14. GATAD2A-deficiency Reactivates Fetal Hemoglobin Synthesis Via Down-regulating MYB And Ameliorates ?-thalassemia Severity
15. High-sensitivity HLA Typing By Saturated Tiling Capture Sequencing(STC-Seq)
16. Preoperative Prediction Of MVI For Early-stage Hepatocellular Carcinoma Based On Circulating Tumor DNA And High-throughput Sequencing
17. Animal Models And Genetic Studies Of Retinal Degeneration Diseases
18. Identification Of TMEM232 Gene Associated With Atopic Dermatitis Through Targeted Capture Sequencing And HaCaT Cells Experiment
19. Analysis Of Gene Mutation In A Hereditary Hearing Loss Family Associated With Vestibular Dysfunction
20. Establishment And Preliminary Application Of New Method For Detection Of Genome Copy Number Variation In Second-generation Sequencing
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