Skip to main content

Table 1 Outcomes of variant and candidate gene identification pipeline in chickpea mutants

From: Defining the mutation sites in chickpea nodulation mutants PM233 and PM405

Sample

Filter Criterion

Total

CDS

Unique

2 Alleles

Read Depth

Min Allele Frequency

Manual IGV Check

PM233

829,368

12,791

412

411

189

168

15

PM405

1,504,184

10,823

133

130

70

48

10

PM638

1,413,448

11,083

133

128

71

48

11

PM665

2,205,449

10,427

138

135

49

44

13

PM796

1,586,765

10,138

90

87

35

23

6

  1. Legend: The listed variant counts are those remaining after implementation of each respective filtration step. The Total column includes all variants found before filtering. The CDS (coding sequence) column includes remaining variants after filtering only for variants found within coding sequence. The Unique column are all variants found only within a single chickpea line. The 2 Alleles column are variants with 2 alelles. The Read Depth column are variants with a read depth of at least 2. The Min Allele Frequency are variants where the alternate allele (the one not matching to the reference sequence) had a frequency of at least 0.9. The Manual IGV (Integrative Genomics Viewer) Check column included variants confirmed after manual confirmation using IGV (i.e. variants which were present in other chickpea lines but not called as variants were excluded)