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Short or low-quality reads, as well as linker and adapter sequences were removed by the Crossmatch program (454 reads, Incogen Inc., Williamsburg, VA, USA) or by the built-in sequence cleanup of Seqman Ngen (Illumina reads, DNAStar, Madison, WI, USA).
They considered the DNA sequence as a digital code of four symbols and speculated that since the integrity of modern information encoding is secured by having error correcting codes built in, DNA sequences might also have such codes to allow repair enzymes to protect the fidelity of nonreplicating DNA and increase the accuracy of replication.
The models were built in the following sequence: (1) univariate models using the primary explanatory variable, etc; and (2) multivariate models which adjusted for potential confounders (age, marital status, income, literacy, district of interview, age of first sexual activity, sex outside the current place of residence and sexual identity).
This place may be empty to start with or marked with "foundation cards," typically the ace of each suit to be built up in sequence to the kings.
The raw 75 bp Solexa reads of the gsNd database were analyzed by the mapping algorithms, Efficient Large scale Alignment of Nucleotide Databases (ELAND), which is built in with the Solexa sequence analysis pipeline of the Illumina sequencer [ 24].
The logic of building an alignment is partially circular: alignments are built in part by maximizing sequence conservation, but then are used to find conserved positions which are, in turn, identified as important.
Several data sets were built in order to calculate the MI for sequence-agonist, sequence-antagonists, sequence-Gi, sequence-Gs and sequence-Gq correlations.
Let { x n } and { y n } be proximal sequences built in such a way that x 0 ∈ A 01, y 0 ∈ A 1, d ( x n + 1, T x n ) = D n 0 and d ( y n + 1, T n y n ) = D n ; ∀ n ∈ Z 0 + and define also the error sequence { x ˜ n } by x ˜ n = y n − x n ; ∀ n ∈ Z 0 +.
After one round of RNA amplification, libraries were built in biological duplicate and sequenced in 100-bp paired-end cycles using the Illumina HiSeq2000 system with SBS technology.
Functional data were acquired using a single shot echo-planar imaging (EPI) sequence with built in motion correction in k-space.
Database URL: https://cghub.ucsc.edu When the first human genome draft sequence was built in the year 2000, its in silico representation was made publicly available as a File Transfer Protocol (FTP) download from the University of California, Santa Cruz (1).
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com