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Next Generation Sequencing Clinical Examples 1.0

Clinical Application 1.0

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Page 1: Clinical Application 1.0

Next Generation SequencingClinical Examples 1.0

In this tutorial we’re going to briefly go through some of the Clinical applications of Next Generation Sequencing and how it can be useful in determining inheritance patterns, distinguishing diagnosis between patients, and assessing the risks of an illness reoccurring.

Page 2: Clinical Application 1.0

Next Generation Sequencing can be used in a variety of places ranging from the clinical setting to a laboratory setting.

Page 3: Clinical Application 1.0

Clinical Example So in this first clinical example is one of [Read Slide]. In this case the 2

brothers have a healthy brother and sister are wondering what the risk is of their own children inheriting the disability. NGS, specif ically Exome Sequencing, was used to determine risk of recurrence in the family

• 22 and 24 year old brothers:– Intellectual Disability– Severe self-injurious behaviors, autistic features– Spastic Diplegia

Page 4: Clinical Application 1.0

Their molecular, cytogenetic, and biochemical conditions were tested and were concluded to be normal .

• Molecular/Cytogenetic:– Karyotype– Fragile X– SNP Chromosome Microarray– Mitochondrial DNA Sequencing– XLMR Panels (>90 genes)

• Biochemical:– Amino acids, organic acids– Lactate, pyruvate– Lysosomal enzyme panel– 7-Dehydrocholesterol– Very long fatty acids

All Results

Normal

Page 5: Clinical Application 1.0

Exome Sequence Results

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Results of Diagnosis

Clinicians were able to:• Determine the inheritance pattern of the

disorder– Autosomal recessive trait, not an X-linked trait

• Determine risk of recurring in healthy siblings– Sister carries the genes, Healthy brother does not.– So it is possible that there could be a recurrence in the family.

Page 7: Clinical Application 1.0

Works Cited

DeFrancesco, Chris. "News Release." Partnership to Deliver Gains in Medical, Dental

Research. N.p., 28 Sept. 2009. Web. 30 June 2014.

<http://today.uchc.edu/newsreleases/2009/sep09/partnership.html>.

Gonzalez, Kelly. "Making Sense of NextGen Sequencing." Ambry Genetics. N.p., n.d.

Web. 27 May 2014.

<http://www.ambrygen.com/sites/default/files/pdfs/NERRG_4-10-

12_Making_Sense_of_NetGen_Sequencing_KG(3).pdf>.

Schug, Jonathan. "Next Generation Sequencing Core." Next Generation Sequencing.

N.p., n.d. Web. 30 June 2014.

<http://www.med.upenn.edu/cores/NextGenerationSequencingCore.shtml>.

"University of Wisconsin–Madison Biotechnology Center." UWBC DNA Sequencing

Facility. N.p., n.d. Web. 30 June 2014.

<http://www.biotech.wisc.edu/services/dnaseq>.