They also include a comprehensive bioinformatics package, enabling you to identify the DNA sequence, clonal prevalence, and V - J family identity
for each gene rearrangement.
As a reagent manufacturer, we offer a comprehensive selection of gel, capillary, and next - generation sequencing PCR assays
for gene rearrangement, chromosome translocation, and gene mutation detection as analyte specific reagents (United States), research use only, or CE - marked in vitro diagnostics to laboratories (outside of North America).
These assays, developed for use with specific Next Generation Sequencing (NGS) platforms, combine optimized, proprietary multiplex PCR master mixes with a software package that converts NGS output data to an easily interpretable form, enabling you to identify the DNA sequence, clonal prevalence, and V - J gene identity
for each gene rearrangement.
Not exact matches
To that end, the US National Center
for Biotechnology Information in Bethesda is developing a database, ClinVar, to integrate clinical and genetic data; others, such as DECIPHER, run by the Sanger Institute, handle genetic data such as chromosome
rearrangements that can disrupt
genes.
After enriching
for CTCs, the researchers analyzed the samples
for ALK
rearrangements and
for an increase in the number of copies of the ALK
gene.
Multiplexed genetic screening
for epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK)
gene rearrangements and subsequent biomarker - guided treatment is cost - effective compared with standard chemotherapy treatment without any molecular testing in the metastatic non-small cell lung cancer (NSCLC) setting in the United States.
Dorothy Romanus, lead author of the study, states «this analysis supports the value of multiplexed testing
for EGFR and ALK
gene rearrangements followed by molecularly - guided therapy in decisions surrounding coverage of related testing and targeted therapy.
Two types of immature B cells, namely fetal liver hybridomas and the leukemic cell line 70Z / 3, both of which have cytoplasmic mu chains but no light chains, were examined
for DNA
rearrangements of their light chain and heavy chain immunoglobulin
genes.
The results suggest that, although the lack of light chain synthesis can be due to a lack of
gene rearrangement, there may also be transcriptional regulation, which may also be important
for the expression of light chain immunoglobulins in immature B cells.
The commercial tests were based on both Sanger sequencing and supplementary testing
for large genomic
rearrangements in both
genes.
They then looked
for DNA breaks associated with receptor
gene rearrangement by using a version of the polymerase chain reaction that amplifies broken DNA.
How these self - promoting
genes jump to these prime locations remains a mystery, but the researchers believe it may have to do with the DNA's three - dimensional structure in particular areas that allows
for genetic
rearrangement when the genome is being copied or when certain
genes are active.
She found,
for example, that by using a technique called the polymerase chain reaction to amplify
genes, she could detect mutations or
rearrangements in cancer - specific
genes in irradiated tissue that had turned cancerous.
Kin Ritchie, Ralph Brinster, and Ursula Storb show that an IgL transgene inhibits
rearrangement of endogenous IgL
genes, providing the first clue
for the mechanism of allelic exclusion of Ig
genes.
Studies on horizontal
gene transfer and enzymemediated DNA
rearrangements lead him to postulate a theory of molecular evolution according to which nature cares actively
for the promotion of biological evolution by using products of specific evolution
genes as well as several intrinsic non-genetic elements.
Duration of Symptoms Does Not Correlate with Results of T - cell
Gene Rearrangement Studies in Patients Evaluated
for Cutaneous T - Cell Lymphoma.
The LymphoTrack ® Dx TRB Assay
for the Illumina MiSeq ® is an in vitro diagnostic product intended
for next - generation sequencing (NGS) based determination of the frequency distribution of TRB
gene rearrangements in patients suspected with having lymphoproliferative disease.
Our NGS kits are used to detect clonal
gene rearrangements, somatic hypermutations and
for the study of MRD.
For example, during T - cell development
genes encoding the TRB molecules are assembled from multiple polymorphic
gene segments that undergo
rearrangements and selection, generating Vb — Db — Jb combinations that are unique in both length and sequence.
Another effort is to identify
genes involved in human development, known as DGAP (Developmental Genome Anatomy Project), which uses naturally occurring human chromosomal
rearrangements in association with major congenital anomalies as the biological reagents
for gene discovery.
-- We have shown that the genetic change causing fibromelanosis is a complex
rearrangement that leads to increased expression of Endothelin 3, a
gene which is known
for promoting the growth of pigment cells, explains Ben Dorshorst the post-doctoral researcher responsible
for the work.
We have been searching
for a mechanism that can explain the genetic cause of majority of BWS and that can provide better understanding of intragenic mutation of p57KIP2 and disruption of KvLQT1
gene by balanced germline chromosomal
rearrangements.
A number of Invivoscribe LymphoTrack Assays, formatted
for use on both the Illumina MiSeq ® and Thermo Fisher Ion PGM ™ platforms, were designed to detect somatic
gene rearrangements within the antigen receptor loci.