Not exact matches
The NB activity in Alberta is far ranging, with such research as self - assembled nanostructures (M. J. Brett), single -
cell cancer
analysis (L. M. Pilarski), computational modeling (D. Wishart), micro-total
analysis systems or lab on a
chip (D. J. Harrison),
cell identification and manipulation (K. Kaler), and microsystems and medical diagnostics (Backhouse).
«Adipose
analysis on microfluidic
chips: Platform works with minute quantities of liquid to grow
cells and study their development.»
For example,
cell culture or biological
analysis, which are conducted in biology laboratories, can be performed on a microfluidic
chip.
RNA from 40 EF, PNP, LE dissected tissues (approximately 250 µm2 each) or ten YFP - expressing control or YFP - and EFTF - expressing animal caps (EFTF - expressing pluripotent
cells) were used for each
chip analysis.
Our technological expertise ranges from the most fundamental approaches to study membrane transport in lymphocytes and dendritic
cells (subcellular compartmentalization, intravital microscopy, phagosomal functions), the systematic
analysis of gene expression and it regulation (RNAseq,
Chip Seq, proteomics) and physiological and pathological immune responses (mouse models for cancer immunity, immunomodulation / vaccination, human clinical studies in cancer).
Current explorations into the molecular underpinnings of
cell circuitry are leveraging multiple data types including expression profiling and epigenetic
analysis leveraging RNA - seq and
CHiP - Seq coupled with molecular markers and cellular phenotypes.
He'd like a way to perform single -
cell analysis using microarrays, instead of full sequencing, but
chip - based bisulfite methods require more nucleic acid — about a microgram — than one
cell can provide.
Genome - wide chromatin interaction
analysis with paired tag sequencing (ChIA - PET) of PolII
CHiP in 5
cell types.
ChIP - Seq
analysis of genome - wide distribution of DAXX in PC3
cells revealed over 59,000 DAXX binding sites, found at regulatory enhancers and promoters.
Chromatin immunoprecipitation and
chip analyses revealed that both active and silenced genes in ES
cells are directly bound by one or more of these three proteins [17], [19].
309/5: 00 Meta -
analysis of rare and common exome
chip variants identifies and replicates S1PR4 and other novel genes influencing blood
cell traits.