Article Friendly article publishing script homepage.
Translate Page To German Tranlate Page To Spanish Translate Page To French Translate Page To Italian Translate Page To Japanese Translate Page To Korean Translate Page To Portuguese Translate Page To Chinese
  Number Times Read : 35     Word Count: 516  
Stats
Total Articles: 83203
Total Authors: 145724
Total Downloads: 13170


Newest Member
Lino Parnell

 
You are at : Home | Diseases

 

Why Preventive Medicine Is Leaning Towards Whole Human Genome Sequencing



[Valid RSS feed]  Category Rss Feed - http://www.medicalsupportforum.com/rss.php?rss=314
By : Brown Harris    29 or more times read
Submitted 2015-03-11 16:07:56
Whole Human Genome Sequencing holds a promising future in clinical practice

Get accurate data analysis and reproducible results within a short time frame with these new approaches that have brought about dramatic changes in the public health sector. Whole human genome sequencing has transformed clinical diagnostics with its widespread screening and high resolution. It allows for easy identification of medically actionable variations for devising effective preventive tools and has decreased the morbidity rate while considerably bringing down the medical costs.

The utility of whole genome sequencing as a diagnostic technique helps in the detection of asymptomatic people who are at the risk of acquiring a preventive disease or disorder and in knowing the carrier status of an individual. From investigating the etiology of a patient and identifying structural variations to evaluating them and interpreting the findings, whole-genome sequencing plays a crucial role in the entire process.

Determine the complete DNA sequence in a single time with Whole Human Genome Sequencing

Whole genome sequencing generates a huge amount of genetic data and by using this data, researchers can design a streamlined approach for quality patient care. This revolutionary technology has accelerated health-care projects while paving the way for personalized patient care. Get high-throughput for clinical research and therapeutic interventions and accurately predict susceptibility towards genetic diseases with whole human genome sequencing. Any given sample even with a negligible amount of DNA can be sequenced and studied for determining its morphological traits and characteristics using this technology. It also facilitates the study of environmental samples in their natural habitat. Whole Human Genome Sequencing has exploded into a variety of uses for medical professionals, researchers, forensic investigators and academicians. From tracing the ancestors and testing genetic predispositions to identifying variations in protein coding patterns and detecting mutations responsible for causing hereditary disorders, through whole genome sequencing every minute detail can be thoroughly investigated and studied. It can accurately determine any alteration and mutation in any given part of the genome and plays a vital part in the early detection and prevention of fatal diseases like cancer, HIV, diabetes, down's syndrome and cystic fibrosis. It has proved to be a powerful tool in exploring the relation between the distinct diseases and human genes. By decoding their different patterns and alterations, doctors can accurately diagnose a number of genetic ailments. It has enabled researchers to overcome all the challenges of time consuming, costly and complicated technologies and allows easy, fast and accurate analysis with a greater yield. Get whole human genome sequencing with DNA quantification kit to identify the risk of developing disease at CD Genomics.

Whole Human Genome Sequencing holds a promising future in clinical practice

Get accurate data analysis and reproducible results within a short time frame with these new approaches that have brought about dramatic changes in the public health sector. Whole human genome sequencing has transformed clinical diagnostics with its widespread screening and high resolution. It allows for easy identification of medically actionable variations for devising effective preventive tools and has decreased the morbidity rate while considerably bringing down the medical costs.
Author Resource:- CD Genomics is among the foremost genome sequencing service providers of the US. Drawing on the unmatched expertise and wide spread experience of its bioinformaticians, the company has garnered the repute of being a reliable and trusted name in the field of genetic research. For more information on DNA diagnostics for hereditary genetic diseases like cancer, log on to cd-genomics.com.
Article From Medical Articles Directory - MedicalSupportForum.com

Related Articles

HTML Ready Article. Click on the "Copy" button to copy into your clipboard.




Firefox users please select/copy/paste as usual
Rate This Article
Vote to see the results!

Do you like this article?
  • Yes.
  • Not Sure.
  • No.
New Members
select
Sign up
select
learn more
Affiliate Sign in
Affiliate Sign In
 
Nav Menu
Home
Login
Submit Articles
Submission Guidelines
Top Articles
Link Directory
About Us
Contact Us
Privacy Policy
RSS Feeds

Actions
Print This Article
Add To Favorites

 
Sponsors