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Supplementary Methods (doc 430K)
Supplementary Methods (doc 430K)

... RIN-adjusted case-control status. Naïve adjustment may therefore result in many genes being falsely reported as statistically significantly differentially expressed, but we do identify only 100 and 11 genes differentially expressed by OCD and ED respectively at FDR < 5% by Equation 3, which is far f ...
Mate-pair, paired ends - molecularevolution.org
Mate-pair, paired ends - molecularevolution.org

... chromatograms) • Base sequence called from flowgrams • Qualities ...
Supplementary Methods and Results Sequencing bias due to
Supplementary Methods and Results Sequencing bias due to

... transcript will tend to have higher aggregate read counts than a short transcript, even if the two have equal expression, as the long transcript has more opportunities for sequences from fragmented reads to appear. Oshlack and Wakefield (2009) demonstrated empirically that the proportion of differen ...
NATIONAL BRAIN RESEARCH CENTRE(NBRC) NH-8, Manesar-122050, HARYANA
NATIONAL BRAIN RESEARCH CENTRE(NBRC) NH-8, Manesar-122050, HARYANA

... Mohr’s salt is prepared in warm distilled water by the reaction of (NH4)2SO4 and: ...
Foundations of Genetics Mendelism
Foundations of Genetics Mendelism

... chromosomes fail to separate during anaphase-1 or anaphase-2. It leads to formation of gametes with n-1 or n+1 chromosomes. So in humans instead of normal 23 chromosomes some gamete may have 22 or 24 chromosomes. On fertilizing a normal gamete they produce individuals with 45 or 47 chromosomes. Thes ...
Study Guide
Study Guide

Brief review of Mendelian
Brief review of Mendelian

... Retardation is more common if the fragile X came from the mother, and is more common in males. Is it sex-linked? The reason for fragility is a much multiplied triplet CGG repeat sequence (usually ~30x, in fragile X 100-1000s of times. Up to ~200 repeats there may be no retardation. But the number o ...
Supplemental Methods and Figure Legends
Supplemental Methods and Figure Legends

... XhoI site was incorporated into the downstream primer for HHT2. The resulting plasmids (pRB633, HHT2; pRB591, HHF2) were used as templates for site-directed mutagenesis using the QuikChange Multi system (Stratagene). P. angusta H3 and H4 each differ from the respective S. cerevisiae proteins at thre ...
Nucleotide sequence of the thioredoxin gene from
Nucleotide sequence of the thioredoxin gene from

Nucleic Acids Research
Nucleic Acids Research

... ERCC-1 cDNA as a probe. To establish whether this clone encoded a functional ERCC-1 protein the cDNA insert of AcDME was released with EcoRI, subcloned in a SV40 based mammalian expression cartridge (see Materials and Methods) and transfected to CHO 433B cells. The results of this experiment, in whi ...
Question 1
Question 1

... Additional Practice ICE #2 Questions ...
Southern Blotting DNA Fingerprinting
Southern Blotting DNA Fingerprinting

... Electrophoresis To do Denaturation/DepurinationTo do Blotting Step To do Probing 2 wks done ...
Protein Synthsis
Protein Synthsis

...  This order is called the reading frame  Changing the reading frame completely changes the resulting ...
Recombinant DNA cloning technology
Recombinant DNA cloning technology

... which react with any molecule. • If a protein is injected into a rabbit (or goat, or sheep, etc.) the blood isolated from the injected animal will have antibodies against the injected protein. • Mono-clonal antibodies are produced from cells grown in tissue culture, and can be “made” to have antibod ...
On the bursting of gene products
On the bursting of gene products

Identification and characterization of the virion protein products of
Identification and characterization of the virion protein products of

The Cell Recorded Lectures
The Cell Recorded Lectures

Teacher Guide
Teacher Guide

Protocol for Phage T1-Resistant TransforMax™ EC100™
Protocol for Phage T1-Resistant TransforMax™ EC100™

Genome-wide Dissections of DNA Damage Induced Transcriptional
Genome-wide Dissections of DNA Damage Induced Transcriptional

... dimensionality of the problem  co-expression → co-function  co-expression → co-regulation • Partition the genes to achieve:  Homogeneity: genes inside a cluster show highly similar expression pattern.  Separation: genes from different clusters have different expression patterns. ...
Bacteria and Archaea Generaliza,ons Three Most Common Shapes
Bacteria and Archaea Generaliza,ons Three Most Common Shapes

... flagella  that  are   structurally  and   func8onally  different   from  eukaryo8c  flagella   •  In  a  heterogeneous   environment,  many   bacteria  exhibit  taxis,  the   ability  to  move  toward  or   away  from  certain  s8muli   ...
Virus identification For virus identification samples of nasal
Virus identification For virus identification samples of nasal

... For virus identification samples of nasal discharge were used. Knowing that this material warrants lower sensitivity than nasopharyngeal aspirate, we chose these samples for compliance reasons since aspiration is associated with some discomfort. The volunteers blew their noses into a cellulose wipe ...
Proximal promoter
Proximal promoter

... • How much is a TF binding site used – Observed expression of all genes – Predicted site count ...
Full Paper - Biotechniques.org
Full Paper - Biotechniques.org

... although not perfectly homologous, still encodes a W-X-X-X-Y amino acid residue. Two of the other segments of the PEX5 gene that encode TPR motifs are fewer than 100bp upstream from the beginning of the 1.2kb sequence reported here. The third is coded by a sequence between bases 840 and 1040 (fig. 3 ...
Supplementary Material
Supplementary Material

... Figure S4: Results from nonnegative matrix factorization. (A) Consensus clustering using four algorithms (nsnmf, offset, lee, brunet, see (Gaujoux, R. & Seoighe, C. A flexible R package for nonnegative matrix factorization. BMC Bioinformatics 11, 367 (2010)) for details) showing cophenetic coefficie ...
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Artificial gene synthesis

Artificial gene synthesis is a method in synthetic biology that is used to create artificial genes in the laboratory. Currently based on solid-phase DNA synthesis, it differs from molecular cloning and polymerase chain reaction (PCR) in that the user does not have to begin with preexisting DNA sequences. Therefore, it is possible to make a completely synthetic double-stranded DNA molecule with no apparent limits on either nucleotide sequence or size. The method has been used to generate functional bacterial or yeast chromosomes containing approximately one million base pairs. Recent research also suggests the possibility of creating novel nucleobase pairs in addition to the two base pairs in nature, which could greatly expand the possibility of expanding the genetic code.Synthesis of the first complete gene, a yeast tRNA, was demonstrated by Har Gobind Khorana and coworkers in 1972. Synthesis of the first peptide- and protein-coding genes was performed in the laboratories of Herbert Boyer and Alexander Markham, respectively.Commercial gene synthesis services are now available from numerous companies worldwide, some of which have built their business model around this task. Current gene synthesis approaches are most often based on a combination of organic chemistry and molecular biological techniques and entire genes may be synthesized ""de novo"", without the need for precursor template DNA. Gene synthesis has become an important tool in many fields of recombinant DNA technology including heterologous gene expression, vaccine development, gene therapy and molecular engineering. The synthesis of nucleic acid sequences is often more economical than classical cloning and mutagenesis procedures.
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