- Convert to SimWalk2 format
- Convert to MENDEL format
- Convert to ASPEX format
- Convert to GeneHunter-Plus format
- Convert to GeneHunter format
- Convert to APM format
- Convert to APM MULT multiple locus
format
- Create nuclear families
- Convert to SLINK format
- Convert to SPLINK format
- Set up for homogeneity analyses
- Convert to SIMULATE format
- Create summary files
- Convert to SAGE format
- Set up for TDTMax analyses
- Convert to SOLAR format
- Convert to Vitesse format
- Convert to Linkage format
- Test loci for Hardy-Weinberg Equilibrium
- Convert to Allegro format
- Convert to MLBQTL format
- Convert to SAGE4.0 format
- Pre-makeped format
- Merlin/SimWalk2-NPL format**
- PREST format
- PAP format
- Merlin format
- LOKI format
- Mendel5 format [New]
** Note that the Merlin/SimWalk2 interface option will
only work with Merlin version 0.10.2 (or higher) and SimWalk2 version 2.89 (or higher), the latest
releases of these two software.
IV - The Analysis menu
After all the input files
and the chromosome number have been specified, then one proceeds to
the Analysis menu, which presents a variety of different conversion
options:
==========================================================
ANALYSIS MENU
==========================================================
1 SimWalk2 format 16 SOLAR format
2 MENDEL format 17 Vitesse format
3 ASPEX format 18 Linkage format
4 GeneHunter-Plus format 19 Test loci for HWE
5 GeneHunter format 20 Allegro format
6 APM format 21 MLBQTL format
7 APM MULT format 22 SAGE 4.0 format
8 Create nuclear families 23 Pre-makeped format
9 SLINK format 24 Merlin/SimWalk2-NPL format
10 SPLINK format 25 PREST format
11 Homogeneity analyses 26 PAP format
12 SIMULATE format 27 Merlin format
13 Create summary files 28 Loki format
14 SAGE format 29 Mendel 5 format
15 TDTMax analyses
Overview:
Note that we can not
provide in depth documentation for each of the programs for which
Mega2 can create files; in fact, we assume that the user will read
the documentation of the appropriate program. Also, since many of
these external programs are written by others, it is possible (and
perhaps likely) that Mega2 will be out of synch with a newly updated
version of one of these programs. If you notice this, please notify
us as soon as possible.
In brief, the various
options in the Analysis menu are listed below. Note that in most
cases, in addition to generating appropriately re-formatted files,
Mega2 also generates a C-shell script that will automatically run the
desired program. However, these C-shell scripts will only function
correctly if the needed programs (with the appropriate names) are in
your path and installed properly on your workstation.
1. Create SimWalk2 format files
This option creates the
files needed for haplotyping, parametric analysis, non-parametric
analysis, or IBD estimation via the SIMWALK2 program.
Name: SIMWALK2 2.82
Primary reference(s): (Sobel and Lange
1996)
2. Convert to MENDEL 3 format
This option creates output files in the
old MENDEL 3 format.
NOTE: This option will
also place the chromosome and map position information into the locus
data file, as required by the RELPAIR program by Michael Boehnke and
William L. Duren (Boehnke and Cox 1997).
Name: MENDEL
Primary reference(s): (Lange et al.
1988)
3. Convert to ASPEX format
This option creates files
in the appropriate format for analysis via the many modules (sib_ibd,
sib_tdt, sib_phase, sib_map) of the ASPEX program. There is an option
to convert larger pedigrees to their component nuclear families if
needed.
Name: ASPEX
Primary reference(s): (Hinds and Risch
1996)
4. Convert to GeneHunter-Plus format
This option creates the
files needed for analysis via the GeneHunter-Plus program.
Name: GeneHunter-Plus
Primary reference(s): (Kong and Cox
1997)
5. Convert to GeneHunter format
This option creates the
files needed for analysis via the GeneHunter program.
Name: GeneHunter
Primary reference(s): (Kruglyak et al.
1996)
6. Convert to APM format
This option creates the
files needed for analysis via the Affected Pedigree Member method
(single marker analyses).
Name: APM and APM Mult
Primary reference(s): (Weeks and Lange
1988)
7. Convert to APM MULT multiple locus format
This option creates the
files needed for analysis via the multilocus version of the Affected
Pedigree member method.
8. Create nuclear families
This option breaks down
larger pedigrees into their component nuclear families (parents plus
children), and output the resulting locus and pedigree files in
LINKAGE format.
9. Convert to SLINK format
This option creates the
files needed for input into the simulation program SLINK.
Name: SLINK, FASTSLINK (Use FASTSLINK
instead of SLINK)
Primary reference(s): (Ott 1989; Weeks et
al. 1990)
10. Convert to SPLINK format
This option creates the
files needed for linkage analyses using affected sib-pairs as
implemented in the SPLINK program by David Clayton.
Name: SPLINK
Primary reference(s): (Holmans 1993)
11. Set up for homogeneity analyses
This option creates the
files needed to compute lod scores under heterogeneity, using
component programs from the ANALYZE package.
Name: ANALYZE package
Primary reference(s): (Terwilliger 1996)
12. Convert to SIMULATE format
This option creates the
files needed for input into the simulation program SIMULATE.
Name: SIMULATE
Primary reference(s): (Terwilliger et al.
1993)
13. Create summary files
This option creates
summary files providing information about the segregation of the
trait, counts of affected relative pairs and affected sibling pairs,
marker allele frequencies (including observed and expected
heterozygosity), genotyping success rate, and phenotype counts summaries.
There is also an option to
create counts of alleles and genotypes within categories (affection
status categories or liability class categories).
The different summary options can be selected using the Summary file
option sub-menu:
Selection Menu: Summary file options
1) Create segregation and relative count summary files.
2) Create allele frequency summary table.
3) Count alleles and genotypes within groups.
4) Create genotyping success rate summary.
5) Create quantitative phenotype summary.
Enter selection: 1 - 5 >
14. Convert to SAGE format
This option creates the
files needed for analysis via the SAGE package. This supports the old
FORTRAN-like SAGE format (rather than the new more elegant format now
available in beta-version).
Name: SAGE
Primary reference(s):
15. Set up for TDTMax analyses
This option creates the
files needed for analysis via the TDTMax program.
Name: TDTMax
Primary reference(s): (Morris et al.
1997)
16. Convert to SOLAR format
This option creates the
files needed for analysis via the SOLAR package.
Name: SOLAR
Primary reference(s): (Blangero and Almasy
1997; Almasy and Blangero 1998)
17. Convert to Vitesse format
This option creates files in LINKAGE format for
analysis with Vitesse. Note that sets up shell-scripts that automate
MLINK-like and LINKMAP-like analyses.
Name: Vitesse
Primary reference(s): (O'Connell and Weeks
1995)
18. Convert to Linkage format
This option creates files in LINKAGE format.
This is useful for reordering loci or selecting subsets of loci from
large files.
Name: LINKAGE
Primary reference(s): (Lathrop and Lalouel
1984; Lathrop et al. 1986; Lathrop and Lalouel 1988)
19. Test loci for Hardy-Weinberg Equilibrium
This option permits one to test markers for
Hardy-Weinberg equilibrium using either the "hwe" program by Guo and
Thompson (1992) or the "Gen" program by Lazzeroni and Lange
(1997).
Name: hwe
Web:
Primary reference(s): (Guo and Thompson
1992)
Name: Gen
Web:
Primary reference(s): (Lazzeroni and Lange
1997)
20. Convert to Allegro format
This option creates the
files needed for analysis via the Allegro program. Further information
is available at the URL below.
Name: Allegro
Primary reference(s):
Allegro, a new computer program for multipoint linkage analysis;
(May 2000, Gudbjartsson DF, Jonasson K, Frigge ML, Kong A)
21. Convert to MLBQTL format
This option creates the
files needed for the analysis of quantitative traits as well as affection status
loci via the Maximum-Likelihood-Binomial extension of the GENHUNTER program.
Please make sure that quantitative data are normalized, as required by the
MLBQTL program.
Name: MLBQTL
Primary reference(s): (Alcais A, Abel L. 1999)
22. Convert to S.A.G.E. 4.0 format
This option creates the
files needed for using the new SAGE 4.0 version. Currently, the user has to
manually add sections required for running various SAGE 4.0 programs to
the bottom of the parameter file. The pedinfo program can be run as is.
Name: S.A.G.E. 4.0 Beta 6a
Primary reference(s):
23) Convert to pre-makeped format
This option will output pedigree
and locus files where the pedigrees are in pre-makeped format. If the
input pedigree file was in a post-makeped format, this option will
also connect together loops in the output.
24. Setup for Merlin-SimWalk2 combined analysis
This option sets up one set
of output data files which can be run through Merlin's NPL analysis option,
and a second set which can be run through SimWlak's NPL option. It also
sets up the requisite scripts that run these two programs in tandem, feeding
in NPL results from Merlin to SimWalk2. To use this option, the latest
versions of Merlin (0.10.2 or higher) and Simwalk2 (2.89 or higher) are required.
Name: Merlin
25. Convert to PREST 3.0 format
This option sets up pedigree,
chromosome, control and script files for analyzing with PREST
(Pedigree RElationship Statistical Test) version 3.0.
Name: PREST 3.0
26. Convert to PAP 5.0 format
This option sets up the files
necessary for running PAP (Pedigree Analysis Package) including the triplets
file (trip.dat), the phenotypes file (phen.dat), the control file
(header.dat), and the locus file (popln.dat).
Name: PAP 5.0
27. Convert to Merlin format
This option sets up the
files necessary for running Merlin including the pedigree,
locus and map files.
Name: Merlin
28. Convert to LOKI format
This option sets up the
files necessary for running LOKI including the pedigree file, control files,
and link files.
Name: Loki version 2.3
29. Convert to MENDEL 5 format
This option sets up the
files necessary for running Mendel5 including the pedigree file, locus, map,
penetrance and control file per chromosome.
Name: Mendel 5.0
Primary reference(s): (Lange et al.
1988)