Provided by: ncbi-tools-bin_6.1.20120620-10_amd64 
NAME
spidey - align mRNA sequences to a genome
SYNOPSIS
spidey [-] [-F N] [-G] [-L N] [-M filename] [-N filename] [-R filename] [-S p/m] [-T N]
[-X] [-a filename] [-c N] [-d] [-e X] [-f X] [-g X] -i filename [-j] [-k filename] [-l N]
-m filename [-n N] [-o str] [-p N] [-r c/d/m/p/v] [-s] [-t filename] [-u] [-w]
DESCRIPTION
spidey is a tool for aligning one or more mRNA sequences to a given genomic sequence.
spidey was written with two main goals in mind: find good alignments regardless of intron
size; and avoid getting confused by nearby pseudogenes and paralogs. Towards the first
goal, spidey uses BLAST and Dot View (another local alignment tool) to find its
alignments; since these are both local alignment tools, spidey does not intrinsically
favor shorter or longer introns and has no maximum intron size. To avoid mistakenly
including exons from paralogs and pseudogenes, spidey first defines windows on the genomic
sequence and then performs the mRNA-to-genomic alignment separately within each window.
Because of the way the windows are constructed, neighboring paralogs or pseudogenes should
be in separate windows and should not be included in the final spliced alignment.
Initial alignments and construction of genomic windows
spidey takes as input a single genomic sequence and a set of mRNA accessions or FASTA
sequences. All processing is done one mRNA sequence at a time. The first step for each
mRNA sequence is a high-stringency BLAST against the genomic sequence. The resulting hits
are analyzed to find the genomic windows.
The BLAST alignments are sorted by score and then assigned into windows by a recursive
function which takes the first alignment and then goes down the alignment list to find all
alignments that are consistent with the first (same strand of mRNA, both the mRNA and
genomic coordinates are nonoverlapping and linearly consistent). On subsequent passes,
the remaining alignments are examined and are put into their own nonoverlapping,
consistent windows, until no alignments are left. Depending on how many gene models are
desired, the top n windows are chosen to go on to the next step and the others are
deleted.
Aligning in each window
Once the genomic windows are constructed, the initial BLAST alignments are freed and
another BLAST search is performed, this time with the entire mRNA against the genomic
region defined by the window, and at a lower stringency than the initial search. spidey
then uses a greedy algorithm to generate a high-scoring, nonoverlapping subset of the
alignments from the second BLAST search. This consistent set is analyzed carefully to
make sure that the entire mRNA sequence is covered by the alignments. When gaps are found
between the alignments, the appropriate region of genomic sequence is searched against the
missing mRNA, first using a very low-stringency BLAST and, if the BLAST fails to find a
hit, using DotView functions to locate the alignment. When gaps are found at the ends of
the alignments, the BLAST and DotView searches are actually allowed to extend past the
boundaries of the window. If the 3' end of the mRNA does not align completely, it is
first examined for the presence of a poly(A) tail. No attempt is made to align the
portion of the mRNA that seems to be a poly(A) tail; sometimes there is a poly(A) tail
that does align to the genomic sequence, and these are noted because they indicate the
possibility of a pseudogene.
Now that the mRNA is completely covered by the set of alignments, the boundaries of the
alignments (there should be one alignment per exon now) are adjusted so that the
alignments abut each other precisely and so that they are adjacent to good splice donor
and acceptor sites. Most commonly, two adjacent exons' alignments overlap by as much as
20 or 30 base pairs on the mRNA sequence. The true exon boundary may lie anywhere within
this overlap, or (as we have seen empirically) even a few base pairs outside the overlap.
To position the exon boundaries, the overlap plus a few base pairs on each side is
examined for splice donor sites, using functions that have different splice matrices
depending on the organism chosen. The top few splice donor sites (by score) are then
evaluated as to how much they affect the original alignment boundaries. The site that
affects the boundaries the least is chosen, and is evaluated as to the presence of an
acceptor site. The alignments are truncated or extended as necessary so that they
terminate at the splice donor site and so that they do not overlap.
Final result
The windows are examined carefully to get the percent identity per exon, the number of
gaps per exon, the overall percent identity, the percent coverage of the mRNA, presence of
an aligning or non-aligning poly(A) tail, number of splice donor sites and the presence or
absence of splice donor and acceptor sites for each exon, and the occurrence of an mRNA
that has a 5' or 3' end (or both) that does not align to the genomic sequence. If the
overall percent identity and percent length coverage are above the user-defined cutoffs, a
summary report is printed, and, if requested, a text alignment showing identities and
mismatches is also printed.
Interspecies alignments
spidey is capable of performing interspecies alignments. The major difference in
interspecies alignments is that the mRNA-genomic identity will not be close to 100% as it
is in intraspecies alignments; also, the alignments have numerous and lengthy gaps. If
spidey is used in its normal mode to do interspecies alignments, it produces gene models
with many, many short exons. When the interspecies flag is set, spidey uses different
BLAST parameters to encourage longer and more gaps and to not penalize as heavily for
mismatches. This way, the alignments for the exons are much longer and more closely
approximate the actual gene structure.
Extracting CDS alignments
When spidey is run in network-aware mode or when ASN.1 files are used for the mRNA
records, it is capable of extracting a CDS alignment from an mRNA alignment and printing
the CDS information also. Since the CDS alignment is just a subset of the mRNA alignment,
it is relatively straightforward to truncate the exon alignments as necessary and to
generate a CDS alignment. Furthermore, the untranslated regions are now defined, so the
percent identity for the 5' and 3' untranslated regions is also calculated.
OPTIONS
A summary of options is included below.
- Print usage message.
-F N Start of genomic interval desired (from; 0-based).
-G Input file is a GI list.
-L N The extra-large intron size to use (default = 220000).
-M filename
File with donor splice matrix.
-N filename
File with acceptor splice matrix.
-R filename
File (including path) to repeat blast database for filtering.
-S p/m Restrict to plus (p) or minus (m) strand of genomic sequence.
-T N Stop of genomic interval desired (to; 0-based).
-X Use extra-large intron sizes (increases the limit for initial and terminal introns
from 100kb to 240kb and for all others from 35kb to 120kb); may result in
significantly longer compute times.
-a filename
Output file for alignments when directed to a separate file with -p 3 (default =
spidey.aln).
-c N Identity cutoff, in percent, for quality control purposes.
-d Also try to align coding sequences corresponding to the given mRNA records (may
require network access).
-e X First-pass e-value (default = 1.0e-10). Higher values increase speed at the cost
of sensitivity.
-f X Second-pass e-value (default = 0.001).
-g X Third-pass e-value (default = 10).
-i filename
Input file containing the genomic sequence in ASN.1 or FASTA format. If your
computer is running on a network that can access GenBank, you can substitute the
desired accession number for the filename.
-j Print ASN.1 alignment?
-k filename
File for ASN.1 output with -k (default = spidey.asn).
-l N Length coverage cutoff, in percent.
-m filename
Input file containing the mRNA sequence(s) in ASN.1 or FASTA format, or a list of
their accessions (with -G). If your computer is running on a network that can
access GenBank, you can substitute a single accession number for the filename.
-n N Number of gene models to return per input mRNA (default = 1).
-o str Main output file (default = stdout; contents controlled by -p).
-p N Print alignment?
0 summary and alignments together (default)
1 just the summary
2 just the alignments
3 summary and alignments in different files
-r c/d/m/p/v
Organism of genomic sequence, used to determine splice matrices.
c C. elegans
d Drosophila
m Dictyostelium discoideum
p plant
v vertebrate (default)
-s Tune for interspecies alignments.
-t filename
File with feature table, in 4 tab-delimited columns:
seqid (e.g., NM_04377.1)
name (only repetitive_region is currently supported)
start (0-based)
stop (0-based)
-u Make a multiple alignment of all input mRNAs (which must overlap on the genomic
sequence).
-w Consider lowercase characters in input FASTA sequences to be masked.
AUTHOR
Sarah Wheelan and others at the National Center for Biotechnology Information; Steffen
Moeller contributed to this documentation.
SEE ALSO
blast(1), <http://www.ncbi.nlm.nih.gov/spidey>