Q. Which of the following is not correct about BLAST?

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Q. If one is looking for protein homologs encoded in newly sequenced genomes, one may use TBLASTN, which translates nucleotide database sequences in all six open reading frames.

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Q. Which of the following is not correct about FASTA?

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Q. The first step in FASTA alignment id to arrange the sequences in matrices’ rows and columns in order to be analyzed.

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Q. The positional difference for each word between the two sequences is obtained by ________ the position of the ______ sequence from that of the _______ sequence and is expressed as the offset.

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Q. The second step in FASTA is to narrow down the high similarity regions between the two sequences.

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Q. In FASTA, neighboring high-scoring segments along the same diagonal are selected and joined to form a single alignment.

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Q. The last step is to perform a statistical evaluation of the final alignment as in BLAST, which produces the E-value.

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Q. The web-based FASTA program is offered by the European Bioinformatics Institute.

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Q. FASTX, which compares a protein query sequence to a translated DNA database.

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Q. FASTA doesn’t use bit scores.

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Q. Z-score describes the number of standard deviations from the mean score for the database search.

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Q. In FASTA, For a Z-score > 15, the match can be considered extremely ______ with _____ of a homologous relationship.

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Q. BLAST uses a _______ to find matching words, whereas FASTA identifies identical matching words using the _____

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Q. Which of the following is not a benefit or a factual of FASTA over BLAST?

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Q. The use of low-complexity masking in the BLAST procedure means that it may have higher specificity than FASTA because potential false positives are reduced.

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Q. Which of the following is not a benefit of BLAST?

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Q. BLAST might not find matches for very short sequences.

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Q. BLAST often produces several short HSPs rather than a single aligned region.

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Q. FASTA is derived from logic of the dot plot.

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