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Cluster Analysis for Gene Expression Data
Cluster Analysis for Gene Expression Data

... In cluster analysis, one wishes to partition a given data set into groups based on given features such that the data points in a group are more similar to each other than points in different groups. There is a very rich literature on cluster analysis going back over three decades. Numerous approache ...
Genomic approaches for the understanding of aging
Genomic approaches for the understanding of aging

... The development of DNA microarray introduced the concept of genomics in biology and presented a valuable and robust tool for the global measurement of gene expression. It is especially useful for the study of complex biological pathways such as aging. In addition, genomic sequence analysis of variou ...
SMN1 - IS MU
SMN1 - IS MU

... The SMN1 and SMN2 have identical gene structure and are 99.9% identical at the sequence level. The essential difference between the two genes is a single nucleotide change in exon 7 (C or T as indicated). This single nucleotide change affects the splicing of the gene. Thus the majority of SMN transc ...
Solid Tumour Section Soft tissue tumors: Alveolar rhabdomyosarcoma in Oncology and Haematology
Solid Tumour Section Soft tissue tumors: Alveolar rhabdomyosarcoma in Oncology and Haematology

... Among ARMS tumors, ~60% are PAX3-FOXO1positive, ~20% are PAX7-FOXO1-positive, and ~20% are fusion-negative. The PAX7-FKHR fusion is often amplified in tumors (70% of PAX7-FKHR-positive cases) whereas the PAX3-FKHR gene fusion is much less frequently amplified in tumors (5% of PAX3-FKHR-positive case ...
Central Dogma of Molecular Biology: The way of diverting
Central Dogma of Molecular Biology: The way of diverting

... number of atoms known in the universe). ...
Variable clinical manifestation of a novel missense mutation in the
Variable clinical manifestation of a novel missense mutation in the

... between family members. The clinical presentation of the novel mutation points towards a malignant (high incidence of sudden death) form of FHC with varying hypertrophy from mild to severe, in particular, asymmetrical septal hypertrophy. An interesting finding is the coronary abnormalities encounter ...
Multiple Sequence Alignment
Multiple Sequence Alignment

... Identify conserved regions and motifs Identify gene families Generates a consensus sequence First step to the study of phylogenetic relationships ...
Document
Document

... provided that a terminal respiratory electron acceptor, such as nitrate, is available in the medium. Furthermore, it has been reported that the anaerobic β-oxidation pathway is mediated by fadJ, fadI and fadK genes, whose transcriptional regulation is independent of FadR control. ...
The Homologous Drosophila Transcriptional Adaptors ADA2a and
The Homologous Drosophila Transcriptional Adaptors ADA2a and

... In Drosophila and several other metazoan organisms, there are two genes that encode related but distinct homologs of ADA2-type transcriptional adaptors. Here we describe mutations of the two Ada2 genes of Drosophila melanogaster. By using mutant Drosophila lines, which allow the functional study of ...
Oral squamous cell carcinoma (OSCC) – molecular, viral and
Oral squamous cell carcinoma (OSCC) – molecular, viral and

... role in the mechanism of the formation of miRNA regulation (the function of miRNAs appears to be in gene regulation). As a result, this leads to an increase in the rate of cell proliferation, include epithelial, from which the majority of oral cancers originate. It has been shown that amplification ...
Leukaemia Section t(5;14)(q33;q32) PDGFRB/TRIP11 Atlas of Genetics and Cytogenetics in Oncology and Haematology
Leukaemia Section t(5;14)(q33;q32) PDGFRB/TRIP11 Atlas of Genetics and Cytogenetics in Oncology and Haematology

... 10 kb fusion transcript (major) and other (minor) transcripts. ...
Full Text  - Genes | Genomes | Genetics
Full Text - Genes | Genomes | Genetics

... away from adjacent genes, were included in the metagene analysis. To estimate gene expression, RNA-seq samples profiled by modENCODE consortium were used for S2 cell and 14–16 hr embryos (Gerstein et al. 2014). FPKM = 1 was used as a threshold for expressed genes. To detect significantly enriched peak ...
DNA and Translation Gene
DNA and Translation Gene

... • Every DNA gene codes for a specific protein • Codon/anticodon match guarantees proper amino acid • Many amino acids link to make one protein ...
Genetics and Precision Medicine
Genetics and Precision Medicine

... have demonstrated how genome medicine in humans can be applied to health management for acute care patients with time-critical morbidity and mortalities. Although the availability of the bioinformatics infrastructure and speed are not yet available in cats as available for humans, the DNA variant da ...
reviews - UO Blogs
reviews - UO Blogs

... Many of the genetic pathways that guide basic developmental processes in vertebrates and invertebrates have remained largely intact during evolution. This has greatly accelerated the analysis of vertebrate development, as insights gained from model genetic systems such as Drosophila melanogaster cou ...
A systemic gene silencing method suitable for high throughput
A systemic gene silencing method suitable for high throughput

... nurtures the young embryo. We have used the homosporous fern Ceratopteris richardii as a model system for studying gametophyte development because Ceratopteris gametophytes are autotrophic, small (~1 mm) and develop rapidly [1]. They can also be manipulated to develop as males or hermaphrodites by t ...
mRNA Export - e
mRNA Export - e

... encoding proteins that mediate such essential emergency responses as DNA repair by homologous recombination and the heat shock response emphasizes the importance of selective mRNA export for cell survival. Whereas THOC2 and THOC5 expression in ES cells are important for the maintenance of pluripoten ...
TA Repeat Polymorphism of the 5-Reductase Gene and Breast Cancer
TA Repeat Polymorphism of the 5-Reductase Gene and Breast Cancer

... bioactive form, dihydrotestosterone, which then transactivates a number of genes. One of these genes encodes for prostate-specific antigen (PSA), a favorable prognostic factor in breast cancer. The 3' untranslated region of the SRD5A2 gene contains either no TA repeats [(TA)0] or 9 [(TA)9] or 18 [(T ...
How to use KAIKObase: An integrated silkworm genome database
How to use KAIKObase: An integrated silkworm genome database

What is a functional genetic polymorphism?
What is a functional genetic polymorphism?

... or biochemical endophenotypes with genetic polymorphisms or sequence variants (following recommendations of the Human Genome Variation Society, “sequence variant” is a more inclusive term than “polymorphism.” However, a common problem has been a lack of consistent association with a given polymorphi ...
PPT - Bioinformatics.ca
PPT - Bioinformatics.ca

... Lab: Gene IDs, Attributes and Networks • Use yeast demo gene list – Learn about gene identifiers – Learn to use Synergizer and BioMart ...
A study of anticipation in families with hereditary non
A study of anticipation in families with hereditary non

... The third gene, hMLH1 (human MutL Homologue 1), was found by analysis of Swedish families and with roughly 250 found mutations. It is said to be the most important gene of all HNPCC-related genes (Lindblom et al. 1993, Peltomaki and Vasen 2004). The function of hMLH1 includes recognition of mismatch ...
Local gene density predicts the spatial position of genetic loci in the
Local gene density predicts the spatial position of genetic loci in the

... territories [7]. Subsequent analyses confirmed this observation and revealed additional features such as differential intrachromosomal gene positioning within one gene family [8]. In some special cases of highly expressed genomic segments, genes were even observed to extend away from chromosome terr ...
Pitfalls in Genetic Association Studies [M.Tevfik DORAK]
Pitfalls in Genetic Association Studies [M.Tevfik DORAK]

... RNA Editing in The Cell – NCBI Online (www) ...
CRISPR/Cas9: Tools and Applications for Eukaryotic Genome Editing
CRISPR/Cas9: Tools and Applications for Eukaryotic Genome Editing

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RNA-Seq



RNA-seq (RNA sequencing), also called whole transcriptome shotgun sequencing (WTSS), is a technology that uses the capabilities of next-generation sequencing to reveal a snapshot of RNA presence and quantity from a genome at a given moment in time.
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