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DeCypherSW™ (Smith-Waterman
and Framesearch)
High-sensitivity sequence
analysis
Smith-Waterman is a well-established algorithm for local sequence alignment. Since 1981, it has been an essential tool for nucleic and protein comparisons due to its ability to guarantee optimal local alignments. But with today's genomic data output from next-generation sequencing platforms, Smith-Waterman software has been eclipsed by faster search tools such as BLAST (at the expense of sensitivity).
However TimeLogic's high performance Smith-Waterman is preferable to BLAST for many genomics search tasks, including:
- Comparing evolutionarily divergent proteins
- Mapping optimal microarray probes within a genome
- Mapping oligos to a reference sequence with high sensitivity
- All-to-all sequence comparisons within a clustering workflow
- Small RNA studies
The Smith-Waterman implementation for the TimeLogic FPGA solutions accelerates dynamic programming
calculations for research groups that demand high
sensitivity and speed.
Smith-Waterman is included with the CodeQuest workstations and is an available module for the DeCypher Enterprise solutions, where it complements the other sequence comparison modules, including Tera-BLAST, HMM, and GeneDetective.
Interleaving alignments across
reading fames
The Smith Waterman algorithm suite includes a comprehensive set of frameshift
tolerant search tools. Framesearch
helps you identify coding sequences in low quality DNA sequences—such
as CE sequence reads, EST and BAC databases—where sequencing errors
and indels introduce shifts in open reading frames. DeCypher’s
powerful acceleration enables the use of these sensitive, dynamic
methods without a large computing infrastructure. Symmetric Frame Independent (a symmetric version of Framesearch) extend frame-tolerance across multiple reading frames in the query and the target.
Smith-Waterman Search Methods
Algorithm |
Query |
Target |
Description |
Applications |
| Smith-Waterman |
NT |
NT |
like BLASTN, more sensitive, allow gaps |
- Minimize cross-hybridization and maximize microarray
specificity
- find and mask repetitive elements
- find regulatory regions
- "No compromise" homology modeling—find global alignments
of your protein sequence to roteins for which structure
is known
|
AA |
AA |
similar to BLASTP but more sensitive, allows gaps |
Double-Affine
Smith-Waterman |
NT |
NT |
SW, allow very long gaps |
- map cDNAs onto genomes, can gap over long introns
|
AA |
AA |
SW, allow very long gaps |
- situations where entire domains are deleted between
otherwise homologous proteins
|
NT |
AA |
SW, allow very long gaps |
- map proteins onto genomes,
can gap over long introns, if in frame
|
| FrameSearch |
NT |
AA |
like BLASTX, more sensitive, can
align across gaps and frameshifts |
- assign tentative functions to EST
- Overcomes limitations in less sensitive gene finding programs
|
| AA |
NT |
like TBLASTN, more sensitive, can align across gaps and frameshifts |
Symmetric Frame
Independent |
NT |
NT |
Solves indel issues with EST and
other low coverage nucleic data by conducting a sensitive protein
domain search between your nucleic query and the nucleic database,
with frame shifting as needed. |
- similar to
TBLASTX, but more sensitive, allows for gaps and frameshifts
|
Custom Benchmarks
Contact us today for a sample Smith-Waterman or Framesearch benchmarks on your data! |