Exact(1)
To avoid such low log-likelihood values, sequences were divided into groups and a separate parameter estimation was performed per group.
Similar(59)
The number of columns is set by the number of discrete values sequenced through.
E values, sequence identity and alignment length for these hits were found to be just below those of the top hits (E value 10−117, sequence identity ≈62% and alignment length of ≈99%).
They normally include quality values, sequence descriptions, etc. and may contain multiple alignments for each sequence.
Peptide Mass Fingerprinting (PMF) interrogation identified (P05412), TRANSCRIPTION FACTOR AP-1 (PROTO-ONCOGENE C-JUN) (P39) (G0S7) using 34 m/z values, sequence coverage: 62%, (score 91).
Besides the explicit target structure features, specific target GC-content valuesequencenconstraintsnts, and newly developed implicit structural constraints are incorporated and presented.
We must note that DNase I hypersensitivity could not be simply viewed as binary property (peaks versus nonpeaks) but rather continuous values (sequencing signals) representing differential chromatin accessibility.
Let be the space of all real valued sequences.
Let w be the set of all real (or complex) valued sequences.
Let X = (X k ) and Y = (Y k ) be two fuzzy real valued sequences.
By, we denote the space of all real or complex valued sequences.
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