71 results on '"targeted sequencing"'
Search Results
2. Cell-Free DNA in Plasma Reveals Genomic Similarity Between Biliary Tract Inflammatory Lesion and Biliary Tract Cancer
3. Targeted nanopore sequencing using the Flongle device to identify mitochondrial DNA variants
4. DNA methylation analysis of the SDC2, SEPT9 and VIM genes in fecal DNA for colorectal cancer diagnosis
5. Development and validation of a 5K low-density SNP chip for Hainan cattle
6. Evidence of Plasmodium vivax circulation in western and eastern regions of Senegal: implications for malaria control
7. Development and verification of a 10K liquid chip for Hainan black goat based on genotyping by pinpoint sequencing of liquid captured targets
8. Mutation landscape in Chinese nodal diffuse large B-cell lymphoma by targeted next generation sequencing and their relationship with clinicopathological characteristics
9. Rare and common coding variants in lipid metabolism-related genes and their association with coronary artery disease
10. Molecular characteristics of tubo-ovarian carcinosarcoma at different anatomic locations
11. primerJinn: a tool for rationally designing multiplex PCR primer sets for amplicon sequencing and performing in silico PCR
12. Targeted sequencing of selected functional genes in patients with wild-type transthyretin amyloidosis
13. Implementation of Nanopore sequencing as a pragmatic workflow for copy number variant confirmation in the clinic
14. Convergent transcriptomic and genomic evidence supporting a dysregulation of CXCL16 and CCL5 in Alzheimer’s disease
15. Frequently mutated genes in predicting the relapse of stage I lung adenocarcinoma
16. Targeted sequencing of the Panicum miliaceum gene space and genotyping of variant sites from population genetics studies, combined in a single assay, as a tool for broomcorn millet assisted breeding
17. DNA methylation profiling of meningiomas highlights clinically distinct molecular subgroups
18. Low-density AgriSeq targeted genotyping-by-sequencing markers are efficient for pedigree quality control in Pinus taeda L. breeding
19. Molecular characterization of triple-negative myeloproliferative neoplasms by next-generation sequencing
20. Targeted genome-wide SNP genotyping in feral horses using non-invasive fecal swabs
21. Targeted next-generation sequencing of circulating free DNA enables non-invasive tumor detection in myxoid liposarcomas
22. Genetic variants associated with the occurrence and progression of adolescent idiopathic scoliosis: a systematic review protocol
23. Targeted Identification of Rice Grain-Associated Gene Allelic Variation Through Mutation Induction, Targeted Sequencing, and Whole Genome Sequencing Combined with a Mixed-Samples Strategy
24. An efficient CRISPR-Cas9 enrichment sequencing strategy for characterizing complex and highly duplicated genomic regions. A case study in the Prunus salicina LG3-MYB10 genes cluster
25. Identification of TSC2 mosaic mutation limited to cortical tuber with TSC targeted sequencing: a case report and literature review
26. A Panel-Based Sequencing Analysis of Patients with Paget’s Disease of Bone Suggests Enrichment of Rare Genetic Variation in regulators of NF-κB Signaling and Supports the Importance of the 7q33 Locus
27. Molecular profiling of pediatric meningiomas shows tumor characteristics distinct from adult meningiomas
28. Molecular predictors of the outcome of paclitaxel plus carboplatin neoadjuvant therapy in high-grade serous ovarian cancer patients
29. Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders
30. Development of Philadelphia chromosome-negative acute myeloid leukemia with IDH2 and NPM1 mutations in a patient with chronic myeloid leukemia who showed a major molecular response to tyrosine kinase inhibitor therapy
31. Germline and Somatic Mutations in Archived Breast Cancer Specimens of Different Subtypes
32. Combining targeted sequencing and ultra-low-pass whole-genome sequencing for accurate somatic copy number alteration detection
33. Post-mortem genetic investigation of cardiac disease–associated genes in sudden infant death syndrome (SIDS) cases
34. Acquired mutations and transcriptional remodeling in long-term estrogen-deprived locoregional breast cancer recurrences
35. Characterization of genomic alterations in Chinese colorectal cancer patients with liver metastases
36. Genetic investigation of 211 Chinese families expands the mutational and phenotypical spectra of hereditary retinopathy genes through targeted sequencing technology
37. Novel high-resolution targeted sequencing of the cervicovaginal microbiome
38. Targeted sequencing of NOTCH signaling pathway genes and association analysis of variants correlated with mandibular prognathism
39. Targeted sequencing analysis of PPARG identifies a risk variant associated with obstructive sleep apnea in Chinese Han subjects
40. Targeted Sequencing for Studying Economically Useful Traits and Phylogenetic Diversity of Ancient Sheep
41. Liquid Biopsy by Next-Generation Sequencing: a Multimodality Test for Management of Cancer
42. Targeted Sequencing Analysis of the Leptin Receptor Gene Identifies Variants Associated with Obstructive Sleep Apnoea in Chinese Han Population
43. Genetic Variation in RIN3 in the Belgian Population Supports Its Involvement in the Pathogenesis of Paget’s Disease of Bone and Modifies the Age of Onset
44. Targeted sequencing with a customized panel to assess histological typing in endometrial carcinoma
45. Establishment and characterization of a novel dedifferentiated chondrosarcoma cell line, NCC-dCS1-C1
46. Applications of Next Generation Sequencing in Haematological Disorders—Indian Status: Updates from ISHBT 2018
47. The Epidome - a species-specific approach to assess the population structure and heterogeneity of Staphylococcus epidermidis colonization and infection
48. Mutational profiling of micro-dissected pre-malignant lesions from archived specimens
49. Utility of a custom designed next generation DNA sequencing gene panel to molecularly classify endometrial cancers according to The Cancer Genome Atlas subgroups
50. Clinical and mutational profiles of adult medulloblastoma groups
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.