Cargando…

Rare variants: data types and analysis strategies

Detalles Bibliográficos
Autores principales:	Goswami, Chayanika, Chattopadhyay, Amrita, Chuang, Eric Y.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	AME Publishing Company 2021
Materias:	Editorial
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267277/ https://www.ncbi.nlm.nih.gov/pubmed/34277761 http://dx.doi.org/10.21037/atm-21-1635

Ejemplares similares

Role of artificial intelligence in integrated analysis of multi-omics and imaging data in cancer research
por: Phan, Nam Nhut, et al.
Publicado: (2019)

Overcoming the challenges of imputation of rare variants in a Taiwanese cohort
por: Chattopadhyay, Amrita, et al.
Publicado: (2020)

Targeting the gut microbiome for non-communicable diseases: present and future
por: Shivani, Subhashree, et al.
Publicado: (2021)

CLIN_SKAT: an R package to conduct association analysis using functionally relevant variants
por: Chattopadhyay, Amrita, et al.
Publicado: (2022)

A non-threshold region-specific method for detecting rare variants in complex diseases
por: Hsieh, Ai-Ru, et al.
Publicado: (2017)

Development of a Gene-Based Prediction Model for Recurrence of Colorectal Cancer Using an Ensemble Learning Algorithm
por: Chan, Han-Ching, et al.
Publicado: (2021)

Tuberculosis Verrucosa Cutis Developing Over A Keloid: A Rare Presentation
por: Kala, Sanjay, et al.
Publicado: (2010)

Attention Should be Drawn to Rare Diseases and Interpretation of Sequence Variants
por: Tang, Bei-Sha
Publicado: (2016)

Rare Genetic Variants Provide Protection for Obstructive Sleep Apnea
por: Pack, Allan I., et al.
Publicado: (2022)

Undiagnosed Rare Genetic Disorders: Importance of Functional Characterization of Variants
por: Umair, Muhammad, et al.
Publicado: (2023)

VariED: the first integrated database of gene annotation and expression profiles for variants related to human diseases
por: Lee, Chien-Yueh, et al.
Publicado: (2019)

Rare variants analysis using penalization methods for whole genome sequence data
por: Yazdani, Akram, et al.
Publicado: (2015)

Developing treatment strategies for rare cancers
por: Atkinson, Jennifer M., et al.
Publicado: (2011)

Defining the Genetic Landscape of Idiopathic Pulmonary Fibrosis: Role of Common and Rare Variants
por: Moss, Benjamin J., et al.
Publicado: (2023)

Evaluating methods for the analysis of rare variants in sequence data
por: Luedtke, Alexander, et al.
Publicado: (2011)

Using Big Data to Understand Rare Diseases
por: Park, Jun-Bean
Publicado: (2021)

Microfilaria in cytological smears at rare sites coexisting with unusual pathology: A series of seven cases
por: Pantola, Chayanika, et al.
Publicado: (2012)

A major milestone for Translational Cancer Research: indexing in PubMed/PubMed Central
por: Chuang, Eric Y.
Publicado: (2022)

Analytical Modeling of Sensitivity Parameters Influenced by Practically Feasible Arrangement of Bio-Molecules in Dielectric Modulated FET Biosensor
por: Das, Rahul, et al.
Publicado: (2022)

Leveraging well-annotated databases for deep learning in biomedical research
por: Phan, Nam Nhut, et al.
Publicado: (2020)

Potential treatment strategy for the rare osimertinib resistant EGFR L718Q mutation
por: Kawase, Akikazu, et al.
Publicado: (2022)

An adaptive strategy for association analysis of common or rare variants using entropy theory
por: Li, Yu-Mei, et al.
Publicado: (2017)

Mechanisms and the strategy for remission of type 2 diabetes mellitus
por: Chang, Tien‐Jyun
Publicado: (2023)

The end or the start of understanding the genetics of type 2 diabetes
por: Chuang, Lee‐Ming
Publicado: (2010)

Improved power by collapsing rare and common variants based on a data-adaptive forward selection strategy
por: Dai, Yilin, et al.
Publicado: (2011)

Comparing strategies for combined testing of rare and common variants in whole sequence and genome-wide genotype data
por: Malzahn, Dörthe, et al.
Publicado: (2016)

Assessing the impact of missing genotype data in rare variant association analysis
por: Mägi, Reedik, et al.
Publicado: (2011)

COVID-19 pandemic: the delta variant, T-cell responses, and the efficacy of developing vaccines
por: Biswas, Biswajit, et al.
Publicado: (2022)

Comparison of similarity-based tests and pooling strategies for rare variants
por: Zakharov, Sergii, et al.
Publicado: (2013)

Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes
por: Bonàs-Guarch, Sílvia, et al.
Publicado: (2018)

Policies and strategies to facilitate secondary use of research data in the health sciences
por: Burton, Paul R, et al.
Publicado: (2017)

School-Based Suicide Prevention Strategy: Evidence-Based Data and Challenges
por: Kweon, Yong-Sil
Publicado: (2020)

Rethinking glioma treatment strategy
por: Ozawa, Tatsuya, et al.
Publicado: (2014)

Steps Toward the Meaningful Translation of Prevention Strategies for Type 2 Diabetes
por: Cefalu, William T.
Publicado: (2012)

Strategies to Reduce the Cost of Renal Complications in Patients With Type 2 Diabetes
por: Gilmer, Todd P., et al.
Publicado: (2011)

Examining rare side effects in pooled trial data: symptomatic osteonecrosis in Hodgkin lymphoma
por: Borchmann, Sven, et al.
Publicado: (2018)

Nucleic acid vaccination strategies for ovarian cancer
por: Saha, Chayanika, et al.
Publicado: (2022)

A generalized least-squares framework for rare-variant analysis in family data
por: Li, Dalin, et al.
Publicado: (2014)

Longitudinal data analysis for rare variants detection with penalized quadratic inference function
por: Cao, Hongyan, et al.
Publicado: (2017)

Special issue on COVID-19 data integration opportunities and vaccine development strategies
por: Allmer, Jens
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_fhppv25libf6pfed0jghcmqq8h