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High Throughput Screening of Single Nucleotide Polymorphisms
High Throughput Screening of Single Nucleotide Polymorphisms

Linkage Mapping of the ACE I Gene in Pig Vincent Nguyen
Linkage Mapping of the ACE I Gene in Pig Vincent Nguyen

... amplified fragment. The restriction enzyme AluI was used to perform PCR-RFLP test on this SNP in the Berkshire x Yorkshire Resource Family. The genotypes were used to linkage map this loci using CRIMAP. The results showed that ACE is located between microsatellite markers S0229 and SW874 on pig chro ...
KOD -Plus
KOD -Plus

... including without limitation reporting the results of purchaser's activities for a fee or other commercial consideration, is conveyed expressly, by implication, or by estoppel. This product is for research use only. Diagnostic uses under Roche patents require a separate license from Roche. Further i ...
PCR amplification of the bacterial genes coding for nucleic acid
PCR amplification of the bacterial genes coding for nucleic acid

...  the primer pairs in use anneal with highly conserved regions of the Citrobacter freundii (Cf) 16S-rRNA gene  the primer pairs in use will lead to a PCR amplification product of either 256 base pairs (fw1/rv1) or 700 base pairs (fw3/rv2) - your instructor will tell you in the lab which primer pair ...
Item 6 - NHS England
Item 6 - NHS England

... 22. Despite the successes there is still more to be done to fully establish the application of genomic technologies (not just whole genome sequencing) across the whole of the NHS and ensure equitable access. This is particularly in primary care where new molecular point of care testing devices could ...
Rhom-2 Expression Does Not Always Correlate With
Rhom-2 Expression Does Not Always Correlate With

... ern blot was prepared using BamHI-digested DNA. Hybridization of the Southern blot with a TCR-p probez4is shown in Fig 1A. As controls, DNAs from the KB and HPB cell lines were included. A germline band of 23 kb and two smaller rearranged bands for the TCR-p gene were observed for the Kl3 and HPB ce ...
Chromosome Analysis Suite 3.1 (ChAS 3.1)
Chromosome Analysis Suite 3.1 (ChAS 3.1)

... 96 DNA samples from blood of phenotypically healthy male and female individuals obtained from BioServe Biotechnologies The samples in this set were chosen to have been run by different operators and with different kits and reagents while still covering all the HapMap cell line ethnic groups, plus t ...
PDF
PDF

... ABSTRACT: β-Lactoglobulin (β-LG) is the dominant non-casein whey protein found in milk of bovine and of most ruminants. The amino acid sequence of β-LG along with its 3-dimensional structure illustrates linkage with the lipocalin superfamily. Preliminary studies in goats indicated that milk yield ca ...
Pedigree vs. Genomic Inbreeding
Pedigree vs. Genomic Inbreeding

... The effect of inbreeding is dependent on what part of the DNA is inherited from the common ancestor ...


... level is becoming increasingly possible rapidly. By the SNP(Single Nucleotide Polymorphism) technique appear differently between the traits is increasing interested in genetic variation. In case of beef cattle industry DNA markers are available commercially. Thus, in Korean cattle(Hanwoo) the suffic ...
PDF file
PDF file

... • Genome-wide association analysis ...
Acquired Copy Number Alterations in Adult Acute Myeloid Leukemia
Acquired Copy Number Alterations in Adult Acute Myeloid Leukemia

... recurrence. Log2 ratio dot plots of paired tumor and normal DNA research samples from the same individual were generated from data obtained from the Affymetrix Genome-Wide SNP 6.0 arrays (top plot of each panel) and custom NimbleGen CGH 12 ≤135K array data (bottom plot of each panel). Solid horizont ...
Array Differences in Genomic Coverage and Data Quality Impact
Array Differences in Genomic Coverage and Data Quality Impact

... In addition to loss of coverage, discordant calls have the potential to negatively impact GWAS results in other ways. While achieving the highest possible call rate is desirable, including questionable calls at the expense of accuracy can quickly compromise the integrity of the results. The evidence ...
ppt
ppt

... Now we can do it in a week for <$2,000 ...
Add Health Biomarker - Carolina Population Center
Add Health Biomarker - Carolina Population Center

... of biological samples. These biological samples permitted the identification of individuals with sexually transmitted infections [STI] (including HIV), and genotype ascertainment for pairs of full-siblings or twins who resided in the same households. The STI testing allows for analyses of individual ...
Genomics I - Faculty Web Pages
Genomics I - Faculty Web Pages

... SNPs STS ...
Genomics I
Genomics I

... SNPs STS ...
High-throughput genotyping
High-throughput genotyping

... • International collaboration to create a map of human genetic variation • The map is based on common haplotype patterns • Includes information on • SNPs (location, frequency, sequence) ...
- Lab Fabiana Perocchi
- Lab Fabiana Perocchi

... Quantitative estimation of allele-specific expression Accurate estimation of allele-specific expression was achieved by using both specific and common probes, with the intensities of the latter reflecting the total expression of the two alleles (Figure 1B). One main challenge was accounting for off- ...
Infectious Bursal Disease Virus (IBDV)
Infectious Bursal Disease Virus (IBDV)

... and mortality generally at 3 to 6 weeks of age. The disease was first discovered in Gumboro, Delaware in 1962. It is economically important to the poultry industry worldwide due to increased susceptibility to other diseases and negative interference with effective vaccination. In recent years, very ...
Dow, Graham: The limitation of genome wide association studies
Dow, Graham: The limitation of genome wide association studies

... generations
 ago,
 and
 spread
 throughout
 human
 genealogy
 either
 through
 genetic
 drift
 or
 selection.
 
 Rare
 SNPs,
 on
 the
 other
 hand,
 have
 arisen
 from
 recent
 mutations,
 even
 some
 within
the
current
generation,
with
little
time
to
spread.
These
SNPs
are
also
the
basis
for
 genom ...
Using metaMA for differential gene expression analysis from
Using metaMA for differential gene expression analysis from

... in public microarray databases. pvalcombination(esets, classes) method combines p-values from different datasets (esets) to extract differentially expressed genes between two conditions (e.g. healthy, ill) coded by 0 or 1 for each biological sample in (classes). esets a is list of matrices which con ...
Whole genome sequencing and assembly of an avian genome, the
Whole genome sequencing and assembly of an avian genome, the

... put together into a single continuous sequence of DNA using a computer program called “Genome assembler”. The genome assembler looks for overlapping regions between the sequenced fragments and makes use of this information to place the different fragments with respect to each other. This method of g ...
Introduction to DNA Microarrays
Introduction to DNA Microarrays

... – When a cell is making a protein, it translates the genes (made of DNA) which code for the protein into RNA used in its production – The RNA present in a cell can be extracted – If a gene has been expressed in a cell ...
Molecular Cloning of engrafted: A Gene Involved in the
Molecular Cloning of engrafted: A Gene Involved in the

... the region proximal to the ensF3~. The entry clones were then used to isolate a series of overlapping clones extending from the two ends toward the middle of the deletion. Comparison of restriction digests and hybridization analyses indicated when the two separate walks overlapped. A total of 225 kb ...
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Molecular Inversion Probe



Molecular Inversion Probe (MIP) belongs to the class of Capture by Circularization molecular techniques for performing genomic partitioning, a process through which one captures and enriches specific regions of the genome. Probes used in this technique are single stranded DNA molecules and, similar to other genomic partitioning techniques, contain sequences that are complementary to the target in the genome; these probes hybridize to and capture the genomic target. MIP stands unique from other genomic partitioning strategies in that MIP probes share the common design of two genomic target complementary segments separated by a linker region. With this design, when the probe hybridizes to the target, it undergoes an inversion in configuration (as suggested by the name of the technique) and circularizes. Specifically, the two target complementary regions at the 5’ and 3’ ends of the probe become adjacent to one another while the internal linker region forms a free hanging loop. The technology has been used extensively in the HapMap project for large-scale SNP genotyping as well as for studying gene copy alterationsand characteristics of specific genomic loci to identify biomarkers for different diseases such as cancer. Key strengths of the MIP technology include its high specificity to the target and its scalability for high-throughput, multiplexed analyses where tens of thousands of genomic loci are assayed simultaneously.
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