The phrase "a given target sequence" is correct and usable in written English.
It can be used in contexts such as scientific research, programming, or any field where specific sequences or patterns are being discussed.
Example: "In our experiment, we focused on analyzing a given target sequence to determine its genetic variations."
Alternatives: "a specified target sequence" or "a particular target sequence".
For a given target sequence, FINDSITE identifies ligand-bound template structures from a set of distantly homologous proteins recognized by the PROSPECTOR_3 threading approach and superposes them onto the target's structure using the TM-align structural alignment algorithm.
For a given target sequence, ANGLOR first generates multiple sequence alignments by searching through a non-redundant sequence database.
Pools of repeated sequences were obtained by analysis using BLASTN in which a given target sequence was used as both query and subject sequence.
Cross hybridization of homologous probes to a given target sequence on the microarray may also be a contributing factor, especially in comparison to other, more gene-specific measurement techniques [ 35].
However, a small M2 sample may be biased and contain too large a proportion of wild-type DNA which would then prevent a given target sequence containing a mutation from being detected among 8-fold pooled DNAs, depending on the limit for robust mutation detection.
For a given target, it first threads the sequence through the PDB library to identify homologous and analogous templates.
For a given target secondary structure and candidate sequence, the ensemble defect is the average number of incorrectly paired nucleotides at equilibrium evaluated over the ensemble of unpseudoknotted secondary structures.
"Coverage" displays the percentage of positions in a given target having 10 or more overlapping sequence reads, or 20 or more overlapping sequence reads.
Sequences with similarity to a given target nrFLcDNA were grouped into a multi-sequence group.
Graf and coworkers expanded on these results by developing a probe uniqueness score (U) based on the number of unique substrings of sequence within a given target region[22].
Before considering an inverse folding algorithm into specific RNA structures one has to have at least some rationale as to why there exists one sequence realizing a given target as mfe-configuration.
