Now That Whole Genome Sequencing Has Arrived, What Does the Data Really Tell Us?Lampel, Keith
Patient choice consent for whole genome sequencing (WGS) through the Genomic Medicine Service in England covers consent to diagnostic testing and an invitation to the National Genomic Research Library (NGRL). Little is known about what consent conversations for WGS look like in practice. We audio-...
The finished version of the human genome sequence was published in April 2003. This version, which is available to the public, provides nearly all the information needed to do research on the whole human genome, which in turn enables us to better understand the genetic ba...
Assay Time2 hours 30 minutes AMPINEXT™ DNA Size Selection Kit ENZ-GEN506 A complete set of optimized reagents for quick removal of DNA fragments of <150 bps for library preparation in next generation sequencing applications. Assay Time30 minutes...
From single gene to whole genome variations Genetic testing is widely used to diagnose monogenic diseases, such as cystic fibrosis or sickle cell disease, caused by mutations in a single gene. These tests can also identify unaffected carriers of disease-associated genes, allowing them to make infor...
There is the urgent need for therapeutic agents that are effective, affo... EO Ogbadoyi,AO Abdulganiy,TZ Adama,... - 《Journal of Ethnopharmacology》 被引量: 87发表: 2007年 Whole-genome sequencing of Trypanosoma brucei reveals introgression between subspecies that is associated with virulence....
4. Role of whole genome sequencing in drug-resistant tuberculosis management 5. Limitations and challenges to implementation of whole genome sequencing for drug-resistant tuberculosis management 6. Framework for implementation of whole genome sequencing in South Africa 7. Conclusion Ethical statement Conflic...
Whole genome sequencing is a laboratory process that examines a person's DNA makeup in order to provide information about the risk for developing diseases in the future, as well as to diagnose active symptoms or diseases. Currently, the technology is most commonly used to find a medical cause...
F Reed Johnson PhDKaren V MacDonald MPHAmy Pugh BAMichael P Douglas MSKathryn A Phillips PhDGenetics in MedicineMarshall DA, Gonzalez JM, Johnson FR, MacDonald KV, Pugh A, Douglas MP, et al. What are people willing to pay for whole-genome sequencing information, and who decides what...
Although the line between these categories is already blurry, and may ultimately disappear as whole-genome sequencing becomes widely available, we believe that the distinction is still useful with respect to current genetic susceptibility tests. The former "traditional" tests are either essen- tially ...