Vamsi Veeramachaneni
ScholarGPS® ID: 27702060113660
Affiliation History
Field
Life Sciences
Discipline
Genetics
Metrics Summary
Publication Count
22
Predicted Citations
540
Predicted h-index
10
Ranking
Publications and Citation History
Publications based on Top Specialties
Types of Publication
- Publications
- Books
- Patents
- NIH/NSF
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A blood-based screening test for colorectal cancer (CRC) using methylation sequencing. (journal article) Journal of Clinical Oncology, volume 42, issue 16_suppl, pages e15089-e15089 (2024). |
An analysis of likely germline events by tumor tissue testing on large somatic panels. (journal article) Journal of Clinical Oncology, volume 42, issue 16_suppl, pages e22524-e22524 (2024). |
Development of a Low-cost NGS Test for the Evaluation of Thyroid Nodules (journal article) Indian Journal of Surgical Oncology, volume 13, issue 1, pages 17-22 (2022). |
Validation of whole genome sequencing from dried blood spots (journal article) BMC Medical Genomics, volume 14, issue 1 (2021). |
Determining Cost-Optimal Next-Generation Sequencing Panels for Rare Disease and Pharmacogenomics Testing (journal article) Clinical Chemistry, volume 67, issue 8, pages 1122-1132 (2021). |
Ultrasensitive detection of tumor‐specific mutations in saliva of patients with oral cavity squamous cell carcinoma (journal article) Cancer, volume 127, issue 10, pages 1576-1589 (2021). |
Data Analysis in Rare Disease Diagnostics (journal article) Journal of the Indian Institute of Science, volume 100, issue 4, pages 733-751 (2020). |
Patent Number: 10734117 (2020) |
Analysis of solid tumor mutation profiles in liquid biopsy (journal article) Cancer Medicine, volume 7, issue 11, pages 5439-5447 (2018). |
Detection of high frequency of mutations in a breast and/or ovarian cancer cohort: implications of embracing a multi-gene panel in molecular diagnosis in India (journal article) Journal of Human Genetics, volume 61, issue 6, pages 515-522 (2016). |
Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort. (journal article) Molecular vision, volume 22 (2016). |
Release of (and Lessons Learned from Mining) a Pioneering Large Toxicogenomics Database (journal article) Pharmacogenomics, volume 16, issue 8, pages 779-801 (2015). |
Screening of an Indian cohort with breast and/or ovarian cancer by a next-generation sequencing-based panel to detect a high frequency of mutations. (journal article) Journal of Clinical Oncology, volume 33, issue 15_suppl, pages e12505-e12505 (2015). |
Clinical utility of profiling somatic alterations in Indian cancer patients using a multi-gene next generation sequencing (NGS) test. (journal article) Journal of Clinical Oncology, volume 33, issue 15_suppl, pages e22127-e22127 (2015). |
Analytical validation of StrandAdvantage solid tumor NGS test. (journal article) Journal of Clinical Oncology, volume 33, issue 15_suppl, pages e12539-e12539 (2015). |
Targeted deep sequencing of solid tumors to predict response to therapy: A study in an Indian population. (journal article) Journal of Clinical Oncology, volume 32, issue 15_suppl, pages e22059-e22059 (2014). |
Next-Generation Sequencing of Human Mitochondrial Reference Genomes Uncovers High Heteroplasmy Frequency (journal article) PLoS Computational Biology, volume 8, issue 10, pages e1002737- (2012). |
Comparative Methods for Sequence Assembly (book chapter) In Handbook of Computational Molecular Biology Chapman and Hall/CRC (2005) |
Eighty percent of proteins are different between humans and chimpanzees (journal article) Gene, volume 346 (2005). |
DED: Database of Evolutionary Distances (journal article) Nucleic Acids Research, volume 33, issue Database issue, pages D442-D446 (2004). |