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syntenic genes
genes located on the same chromosome. have a higher probability of assorting together (if they are less than 50 map units apart) but can still be separated by recombination
what happens to the 9:3:3:1 ratio with linkage?
the ratio is altered. We can detect linkage by generating a heterozygote and crossing it with a homozygous recessive (test cross)

where is evidence of recombination found?
in the areas where reciprocal exchanges between the homologous chromosomes are found
H. Sturtevant
proposed that recombination frequencies could be used as a measure of physical distance between 2 genes

recombinant genes
are less frequent than parental gametes when genes are linked. The frequency of recombinants never exceeds 50% due to independent assortment
parental chromosomes
occur when meiosis produces no cross overs
single and double crossovers
produce a 1:1 parental to recombinant chromosome ratio on average
two-point cross
occurs when two points on a gene cross over.
limitations of two-point gene crosses and distance measurements
- difficult to determine gene order if two genes are close together
- actual distances between genes do not always add up
- pairwise crosses are time and labor consuming
three-point cross
when 3 points on homologous chromosomes cross over. We can testcross a triply-heterozygous F1 with a tester to produce 8 different phenotypes in the offspring. to find out if a crossover event occurred and in what location, compare parent genotype to offspring two genes at a time

what is the formula for determining genetic map distance on a cross?
(#of recombinant genotypes/total #of genotypes)*100

does estimated genetic distance correlate with physical reality?
the order of genes revealed by a genetic map is accurate, but the actual physical distance (amount of DNA) does not always show direct correspondence to genetic distance, especially with double, triple, or more crossovers. There are also recombination hotspots and a 50%limit on observable recombination frequency

linkage group
is synonymous with a chromosome when many genes per chromosome have been mapped
what does the Chi square test pinpoint?
the probability that ratios are evidence of linkage. In other words, how likely genes are to be linked. Deviations from 1:1:1:1 ratio can represent chance event or linkage.
null hypothesis
states that observed values are no different than expected values (AKA no significant results). i.e. there is no linkage in the case of linkage studies vs proof of linkage
how to use chi square test
take (observed - expected)² /expected, then multiply by 100 to get x²
expected is how many offspring you’d expect with a 1:1:1:1 ratio
