Are whole exome and whole genome sequencing approaches cost-effective? A systematic review of the literature

Are whole exome and whole genome sequencing approaches cost-effective? A systematic review of the literature

Veure altres versions (1)

Dades bibliogràfiques
Autors principals:	Schwarze, K, Buchanan, J, Taylor, J, Wordsworth, S
Format:	Conference item
Publicat:	Elsevier 2018

Ítems similars

Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature
per: Schwarze, K, et al.
Publicat: (2018)

Diagnostic value of exome and whole genome sequencing in craniosynostosis
per: Miller, K, et al.
Publicat: (2016)

Whole exome sequencing of a patient with metastatic hidradenocarcinoma and review of the literature
per: Eva Gupta, et al.
Publicat: (2015-02-01)

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies
per: Ormondroyd, E, et al.
Publicat: (2016)

Whole exome sequencing in the rat
per: Julie F. Foley, et al.
Publicat: (2018-06-01)

Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome
per: Michael Rusch, et al.
Publicat: (2018-09-01)

BALSA: integrated secondary analysis for whole-genome and whole-exome sequencing, accelerated by GPU
per: Ruibang Luo, et al.
Publicat: (2014-06-01)

Whole Exome Sequencing in Atrial Fibrillation.
per: Steven A Lubitz, et al.
Publicat: (2016-09-01)

Comparative analysis of whole exome sequencing kits for the canine genome.
per: Jinhee Jang, et al.
Publicat: (2024-01-01)

Genomic Insights Into Sepsis Course Using Whole Exome Sequencing
per: Carlos Flores, et al.
Publicat: (2016-10-01)

Whole-exome sequencing study of hypospadias
per: Zhongzhong Chen, et al.
Publicat: (2023-05-01)

A cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome
per: Claude Bhérer, et al.
Publicat: (2024-02-01)

Benchmarking of human Y-chromosomal haplogroup classifiers with whole-genome and whole-exome sequence data
per: Víctor García-Olivares, et al.
Publicat: (2023-01-01)

Whole exome sequencing in neurogenetic odysseys: An effective, cost- and time-saving diagnostic approach.
per: Marta Córdoba, et al.
Publicat: (2018-01-01)

Identification of genetic variants in a pedigree associated with epilepsy by using whole exome sequencing and whole genome sequencing
per: Qin-Qin Zhang, et al.
Publicat: (2021-06-01)

Evaluation of whole exome sequencing as an alternative to BeadChip and whole genome sequencing in human population genetic analysis
per: Zoltán Maróti, et al.
Publicat: (2018-10-01)

Diagnosis of fetal nemaline myopathy by whole-exome sequencing: case report and review of literature
per: Q.C. Wu, et al.
Publicat: (2020-12-01)

Integrated Whole Exome and Transcriptome Sequencing in Cholesterol Metabolism in Melanoma: Systematic Review
per: Mohammed Mahmoud Nour Eldin, et al.
Publicat: (2024-03-01)

P769: Trio-whole exome and whole genome sequencing in fetal central nervous system anomalies
per: Ariel Gershon, et al.
Publicat: (2024-01-01)

Somatic retrotransposition in human cancer revealed by whole-genome and exome sequencing
per: Helman, Elena, et al.
Publicat: (2014)

Genomic landscape of hepatocellular carcinoma in Egyptian patients by whole exome sequencing
per: Perihan Hamdy Kassem, et al.
Publicat: (2024-08-01)

Computational and Bioinformatics Frameworks for Next-Generation Whole Exome and Genome Sequencing
per: Marisa P. Dolled-Filhart, et al.
Publicat: (2013-01-01)

Genes to therapy: a comprehensive literature review of whole-exome sequencing in neurology and neurosurgery
per: Joecelyn Kirani Tan, et al.
Publicat: (2024-11-01)

Apert's syndrome: Study by whole exome sequencing
per: Anjana Munshi, et al.
Publicat: (2018-06-01)

The Application of Whole−Exome Sequencing in Patients With FUO
per: Wanru Guo, et al.
Publicat: (2022-01-01)

Reconstructing Native American migrations from whole-genome and whole-exome data.
per: Simon Gravel, et al.
Publicat: (2013-01-01)

Beyond the exome: utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases
per: Lama AlAbdi, et al.
Publicat: (2023-12-01)

SEXCMD: Development and validation of sex marker sequences for whole-exome/genome and RNA sequencing.
per: Seongmun Jeong, et al.
Publicat: (2017-01-01)

Whole exome sequencing in energy deficiency inborn errors of metabolism: A systematic review
per: Fatimah Diana Amin Nordin, et al.
Publicat: (2024-09-01)

miRMut: Annotation of mutations in miRNA genes from human whole-exome or whole-genome sequencing
per: Martyna O. Urbanek-Trzeciak, et al.
Publicat: (2022-03-01)

A benchmarking of human mitochondrial DNA haplogroup classifiers from whole-genome and whole-exome sequence data
per: Víctor García-Olivares, et al.
Publicat: (2021-10-01)

Whole-exome sequencing studies of nonfunctioning pituitary adenomas.
per: Newey, P, et al.
Publicat: (2013)

Challenges in whole exome sequencing: an example from hereditary deafness.
per: Asli Sirmaci, et al.
Publicat: (2012-01-01)

Whole-exome sequencing in evaluation of patients with venous thromboembolism
per: Eun-Ju Lee, et al.
Publicat: (2017-07-01)

Opening Pandora's box? Ethical issues in prenatal whole genome and exome sequencing
per: Horn, R, et al.
Publicat: (2017)

Correction: Genomic landscape of hepatocellular carcinoma in Egyptian patients by whole exome sequencing
per: Perihan Hamdy Kassem, et al.
Publicat: (2024-11-01)

Whole exome sequencing identifies genomic alterations in proximal and distal colorectal cancer
per: Ryia-Illani Mohd Yunos, et al.
Publicat: (2019-09-01)

Whole-exome sequencing identifies distinct genomic aberrations in eccrine porocarcinomas and poromas
per: Maya Puttonen, et al.
Publicat: (2025-02-01)

Interpreting whole genome and exome sequencing data of individual gastric cancer samples
per: Daniela Esser, et al.
Publicat: (2017-07-01)

Comparison of whole genome amplification techniques for human single cell exome sequencing.
per: Erik Borgström, et al.
Publicat: (2017-01-01)