Whole Genome Sequencing (WGS) is the most comprehensive test available through Baylor Genetics. It analyzes up to 98% of the human genome, detecting known and potential disease-causing variants that may not be identified on more targeted genetic testing. Additionally, WGS covers both the protein-...
How It Works Whole Genome Sequencing Support Privacy Forever Our Tests Vs Our Competitors 23andMe is a registered trademark of 23andMe, Inc., AncestryDNA is a registered trademark of Ancestry Operations Inc. dba Ancestry, Family Tree DNA is a registered trademark of Gene By Gene, Ltd., ...
Whole-genome sequencing is suitable for the study of disease-specific genomic abnormalities from cfDNA. The Invitrogen Collibri PS DNA Library Prep Kit for Illumina Systems enables consistent and reproducible cfDNA library p...
MGIEasy Whole Genome Bisulfite Sequencing Library Prep Kit provides an efficient and accurate method for genome-wide methylation library construction and sequencing. It can analyze the DNA methylation status at single base level, and thus enable the construction of a fine genome-wide methylation map. ...
xGen whole exome sequencing solution For WES, samples can be prepared using multiple library preparation methods. The xGen whole exome sequencing solution employs thexGen DNA Library Prep Kit EZ, which uses enzymatic fragmentation to shear high-quality DNA samples. This kit uses a TA ligation-base...
Leveraging the ultrahigh-multiplex PCR approach of Ion AmpliSeq technology and the superior accuracy of the new Ion GeneStudio S5 Systems, the Ion AmpliSeq Exome RDY Kit allows for rapid, accurate sequencing of key exonic regions of the genome, going from D...
A total of 0.5 μg of genomic DNA for each sample from the participating individuals of large rosacea families, was utilized as input material for library generation. Libraries for sequencing were produced by the TruSeq Nano DNA HT Sample Prep Kit (Illumina) according to the manufacturer’s...
Frischknecht M, Jagannathan V, Leeb T. Whole genome sequencing con- firms KIT insertions in a white cat. Anim Genet (2015) 46:98. doi:10.1111/ age.12246Frischknecht M, Jagannathan V, Leeb T. Whole genome sequencing confirms KIT insertions in a white cat. Anim Genet. 2014;46(1):98....
Whole Exome Sequencing (WES) uses Next Generation Sequencing methodology to provide targeted sequence information from the coding regions of the genome.
To increase understanding of the genomic landscape of acral melanoma, a rare form of melanoma occurring on palms, soles or nail beds, whole genome sequencing of 87 tumors with matching transcriptome sequencing for 63 tumors was performed. Here we report