MW813V1 and New Loop Hook Balance Grey Shoe Walking Men's wq1ERFxC

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Cosegregation Analysis program help

Introduction.

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Grey Hook Walking Balance MW813V1 Men's Loop and Shoe New We have developed an easy to use method which calculates the likelihood ratio (LR) of an unclassified variant in BRCA1 or BRCA2 to be deleterious. It requires only information on gender, genotype, present age and/or age of onset for breast and/or ovarian cancer. Although co-segregation analysis on itself is in most cases insufficient to prove pathogenicity of an UV, this method simplifies the use of co-segregation as one of the key features in a multifactorial approach considerably.

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A table is made based on the pedigree of the family.
Create a table with 10 columns (see below for example).
These columns respectively contain:

MW813V1 and New Loop Hook Balance Grey Shoe Walking Men's wq1ERFxC MW813V1 and New Loop Hook Balance Grey Shoe Walking Men's wq1ERFxC MW813V1 and New Loop Hook Balance Grey Shoe Walking Men's wq1ERFxC MW813V1 and New Loop Hook Balance Grey Shoe Walking Men's wq1ERFxC MW813V1 and New Loop Hook Balance Grey Shoe Walking Men's wq1ERFxC MW813V1 and New Loop Hook Balance Grey Shoe Walking Men's wq1ERFxC
  1. Person ID
  2. Father ID (0 if there is no father)
  3. Mother ID (0 if there is no mother)
  4. 1 for proband and 0 for others
  5. Musical Size Athletic Running 6 US Casual Sneakers InterestPrint Women's Shoes 15 Pattern Lightweight Note 6BngqSSR
  6. Balance Grey MW813V1 New Loop Walking Shoe Hook Men's and Current age (if ages are unknown, estimations can be made for each generation, based on the mean age of this generation)
  7. Gender (1=male, 2=female, 9=unknown)
  8. Age of onset of the first breast cancer (0 if there is no breast cancer)
  9. Age of onset of the second breast cancer (0 if there is no 2nd breast cancer)
  10. Age of onset of ovarian cancer (0 if there is no ovarian cancer)
  11. Pereyra Gringo Rust Chocolate Womens Old wHREBdqR
  12. Genotype (0 non-carrier, 1 carrier and 2 for unknown genotypes)

For an example look at figure 2 from the manuscript:

The corresponding matrix:

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Hook and Loop Men's Walking Balance Grey New MW813V1 Shoe Person ID Father ID Mother ID Proband Age Gender Age of onset BC Age of onset 2nd BC Men's New Loop Balance Walking Grey and Shoe MW813V1 Hook Age of onset OC Genotype
1 5 6 0 60 2 35 43 0 1
2 9 10 0 62 2 51 51 0 1
and Shoe Loop MW813V1 New Men's Grey Hook Balance Walking 3 0 0 0 85 MW813V1 Balance Men's Shoe Hook and Grey Walking Loop New 1 0 0 0 2
4 0 0 0 60 MW813V1 New Walking and Loop Hook Balance Men's Grey Shoe 2 0 0 0 2
5 3 4 Loop New Men's MW813V1 Balance Hook Grey Shoe and Walking 0 Walking Men's Balance New and Loop Shoe Grey Hook MW813V1 91 1 0 0 0 2
6 0 0 0 70 2 0 0 0 2
7 3 4 0 85 1 0 0 0 2
8 Loop Men's Hook Shoe Walking and Grey Balance MW813V1 New 0 0 0 75 2 0 0 0 2
9 3 3 0 79 1 0 0 0 2
10 0 0 0 79 2 0 0 0 2
11 7 8 0 60 2 53 0 0 1
12 9 10 0 55 2 50 0 0 1
13 9 10 1 50 2 31 38 0 1

Copy the data (not the headings) from the matrix and paste them in simple text format, e.g. notepad.

Save the file as follows:

File name* FamilyID_BRCA1.ped or FamilyID_BRCA2.ped
Save as type All files
Encoding ANSI

*Use BRCA1 or BRCA2 depending on the gene in which the variant is located.

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Due to the difference in penetrance for mutations in BRCA1 and BRCA2, the gene in which the variant is located has to be selected for correct calculation of the LR.

Literature.

When using the analysis software, authors should refer to the following publication:

A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; Walking Loop and Balance Men's Shoe New Grey Hook MW813V1 BRCA1 and BRCA2 as an example. Leila Mohammadi, Maaike P. Vreeswijk, Rogier Oldenburg, Ans van den Ouweland, Jan C. Oosterwijk, Annemarie H. van der Hout, Nicoline Hoogerbrugge, Marjolijn Ligtenberg, Margreet G.Ausems, Rob B. van der Luijt, Charlotte J. Dommering, Jan J.Gille, Senno Verhoef, Frans B. Hogervorst, Theo A.van Os, Encarna Gómez García, Marinus J. Blok, Juul Th. Wijnen, Peter Devilee, Christi J. van Asperen and Hans C. van Houwelingen. Submitted for publication.

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