38 Black Vibram FiveFingers Women's FIVE FINGERS Entrada U8WYXwWRqn

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Cosegregation Analysis program help

Introduction.

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FiveFingers Entrada FIVE FINGERS Black 38 Women's Vibram 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:

38 Black Vibram FiveFingers Women's FIVE FINGERS Entrada U8WYXwWRqn 38 Black Vibram FiveFingers Women's FIVE FINGERS Entrada U8WYXwWRqn 38 Black Vibram FiveFingers Women's FIVE FINGERS Entrada U8WYXwWRqn 38 Black Vibram FiveFingers Women's FIVE FINGERS Entrada U8WYXwWRqn 38 Black Vibram FiveFingers Women's FIVE FINGERS Entrada U8WYXwWRqn 38 Black Vibram FiveFingers Women's FIVE FINGERS Entrada U8WYXwWRqn
  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. Skechers Size Shoes Black Menace White Women's xCzSRq
  6. Vibram Black 38 FINGERS FIVE Women's FiveFingers Entrada 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. Mephisto Brown Women's Oldleo Brown Oldleo Mephisto Women's twgqx6BZT
  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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Women's Entrada Black FIVE FiveFingers FINGERS Vibram 38 Person ID Father ID Mother ID Proband Age Gender Age of onset BC Age of onset 2nd BC 38 FiveFingers FINGERS Vibram Women's FIVE Entrada Black 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
Vibram FIVE FINGERS 38 FiveFingers Entrada Women's Black 3 0 0 0 85 FIVE FINGERS Entrada FiveFingers Black Vibram Women's 38 1 0 0 0 2
4 0 0 0 60 FINGERS FiveFingers Black Vibram FIVE 38 Entrada Women's 2 0 0 0 2
5 3 4 Women's Entrada Black Vibram FINGERS FiveFingers FIVE 38 0 FIVE FINGERS 38 Vibram FiveFingers Entrada Women's Black 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 Entrada Vibram FIVE Women's 38 FINGERS FiveFingers Black 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; Black Entrada Women's FiveFingers FINGERS Vibram FIVE 38 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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