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LAMARC


LAMARC


version 2.1.2b
Lamarc is a program for doing Likelihood Analysis with Metropolis Algorithm using Random Coalescence. Lamarc estimates effective population sizes, population exponential growth rates, a recombination rate, and past migration rates for one to n populations assuming a migration matrix model with asymmetric migration rates and different subpopulation sizes.

Program information

  • written in C++
  • LINUX
  • Mac OSX
  • Windows

Data type handled

  • DNA sequence
  • RNA sequence
  • SNP
  • Microsatellites
  • electrophoretic data

Input Files

LAMARC File Converter:

can convert PHYLIP, RECOMBINE and MIGRATE files to a LAMARC XML file

LAMARC XML file:

  • surrounded by <lamarc> and </lamarc>

Data section:
contains the actual molecular data, and additional information used to interpret it

  • enclosed in <data> tags
  • <region>:
    • divides molecular data into “regions”
    • available genetic information that is closely linked on the same chromosome and has a known map
    • Use multiple regions for data composed of several disconnected bits or bits whose connections are not known
    • region's name: optional name attribute
  • <effective-popsize> (optional):
    • specify a different relative effective population size for each <region>
  • <spacing>:
    • Information about the relative position of segments
  • <block>:
    • Each segment is indicated by this tag
    • give information about the position of the segment itself and the positions of the markers within the segment
    • <length>: indicates the total length of the segment (important for SNPs)
    • <map-position>: gives the position of this segment on an overall map of the region (the point at which sequencing or scanning began)
    • <locations>: a list of marker positions within the region
    • <offset>: the origin of the segment's numbering system with respect to the boundaries of the region
  • <population>:
    • Within each region you can list various populations
    • if you list <population> tags under more than one region, they will be matched by means of their name attributes, so the names are not optional
    • <individual>: represents all the data for that region that comes from a single biological individual (one or more sets). Individuals can have a name attribute (optional)

How to cite

Kuhner, M. K., 2006 “LAMARC 2.0: maximum likelihood and Bayesian estimation of population parameters.” Bioinformatics 22(6): 768-770.

lamarc.1197550747.txt.gz · Last modified: 2008/07/22 13:30 (external edit)