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Genomics is the study of the genomes of organisms. The field
includes intensive efforts to determine the entire DNA sequence of
organisms and fine-scale genetic mapping efforts. It is a
discipline in genetics that applies recombinant DNA, DNA sequencing
methods, and bioinformatics to sequence, assemble, and analyse the
function and structure of genomes. Genomics III - Methods,
Techniques and Applications is the last volume of our Genomics
series.
Chapter 1 presents an overview of exome sequencing technology and
details its use in identification of molecular bases of rare
diseases in human.
Chapter 2 describes and compares different methods of whole genome
amplification (WGA) for replenishing DNA samples for genetic
studies.
Chapter 3 ilustrates the method of whole genome microarray gene
expression profiling and its application to study the treatment
effect of a widely used cardiovascular drug.
Chapter 4 describes a brief history of large-insert libraries and
their utility in exploring organisms with poor genetic and genome
information.
Chapter 5 proposes a bio-molecular approach for the evaluation of
the anaerobic digestion performance.
In Chapter 6, quantitative issues of the transposon-based gene
delivery methods are addressed. Using the "Sleeping Beauty"
transposon system as a prominent example, special detailed focus is
given to copy number determination and to transposon excision
efficiency quantification by real-time PCR based methodologies.
Chapter 7 provides an overview of extraction of a compendium of
sequence and structural features, as well as the methodology for
function prediction based on the techniques from Artificial
Intelligence and Machine learning.
Chapter 8 presents a statistical method and a data mining solution
for the problem of insertion site analysis and characterization of
Alu elements
Chapter 9 investigates how Mutual Information (MI) can be used to
improve methods of predicting functional residues and enhance
structural data to describe the topological properties of amino
acid coevolution networks within a protein and their interactions.
Chapter 10 attempts to validate MLVA to see if it could predict
MRSA clones that were previously characterized by PFGE, MLST, and
staphylococcal cassette chromosome mec (SCCmec) typing and to
establish possible criteria of clustering MLVA patterns, looking
for high concordance levels.
Chapter 11 introduces a web server which allows the user to
perform genome rearrangement analysis using reversals,
block-interchanges (also called generalized transpositions) and
translocations (including fusions and fissions).
Chapter 12 discussed an algorithm which is used to optimally align
simple sequence repeat (microsatellite) regions as they evolve
uniquely through a process called polymerase slippage.
Chapter 13 possesses a background of the RUN domain research with
an emphasis on the interaction between RUN domain protein including
RUFY proteins and small GTPases with respect to the cell polarity
and membrane trafficking.
In Chapter 14, the authors detail recent advances in understanding
mechanisms of gene regulation in Drosophila.
Chapter 15 provides guidelines for human molecular geneticists to
perform genetic screenings using next generation sequencing.
Chapter 16 describes the process that was used to locate and
characterize small group I introns in the rRNA gene locus of fungi.
Chapter 17 summarizes recent insights in the biology of variant
gene transcription in human and murine malaria species and
addresses the molecular mechanisms at work which regulate the
expression of important virulence factors.
Cancer is a broad group of diseases involving unregulated cell
growth, in which cells divide and grow uncontrollably, forming
malignant tumors, and invade nearby parts of the body. Cancer may
also spread to different parts of the body through the lymphatic
system or the bloodstream. "The Research and Biology of Cancer"
discusses some recent advances in cancer research. There are
totally two volumes: Volume I mainly discusses the role of some
important enzymes and proteins in cancer, whereas Volume II
discusses different types of cancers, including head and neck
cancer, oral cancer, kidney cancer, colon cancer, and thyroid
cancer.
Chapter 1 discusses personalised combination therapy targeting
PI3K/Akt, STAT3, ERK, and EGFR signalling pathways which may
provide clinical benefits for patients with HNSCC. Such therapy is
useful because molecular cross-talk between the EGFR and other RTK
signalling pathways through PI3K/Akt, STAT3, and ERK in HNSCCs,
EGFR inhibitors alone may be unable to suppress EGFR downstream.
Chapter 2 describes tissue based LCM, which is a powerful
technique that combines morphology, histopathology, and molecular
biological analysis. The ability of LCM to retrieve specific
populations of interested cells, combined with the analysis of gene
sequencing and gene expression in these sub-population of cells,
has made LCM an critical device in clinical and investigative oral
oncology.
Chapter 3 discussed several aspects about the use of the
Micronucleus Test to identify genetic damage in individuals at
higher risk of developing oral squamous cell carcinoma and
evaluated the malignant transformation potential of precancerous
lesions.
Chapter 4 aims to picture the landscape of metastatic renal cancer
starting from its pathogenesis, molecular markers, prognostic
factors, metastatic potential, with emphasis on the recent
evolution in the treatment of metastatic renal cancer cases.
Chapter 5 discusses skin-level jejunostomy (SLJ) tube placement
technique using the G-tube, which is a safe procedure in patients
with esophageal cancer. It allows the creation of a long-term
feeding jejunostomy.
Chapter 7 offers a comprehensive review of the small bowel
neoplasms, as well as its varied clinical manifestations,
diagnostic challenges and management principles.
Chapter 8 reviews the current research efforts to identify
biomarkers suitable for non-invasive colon cancer screening.
Chapter 9 conducted a pilot study to determine the safety and
feasibility of an early start of chemotherapy after the resection
of colorectal cancer with distant metastases. Chemotherapy usually
starts after 4 weeks of surgical resection of colorectal cancer.
Unfortunately, there is no study on the optimal length of this
delay. A patient may die because postoperative chemotherapy was not
started soon enough and so a metastatic tumor was able to develop
rapidly. This chapter gives a good review of this problem.
Chapter 10 focuses on the putative role of intestinal microbiota
in the development of colorectal cancer, describing his metabolic
functions and relation with diet, and his interaction with host's
immunity and with molecular and morpho-functional activity of
gastrointestinal tract.
Chapter 11 describes an approach used for identification of a
novel PPI. It shows that an uncharacterized protein,
two-transmembrane protein 88 (TMEM88), is a binding partner of
Dishevelled (Dvl/Dsh) by using a combination of techniques,
including bioinformatic, biophysical, and biochemical methods.
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