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@@ -2,8 +2,8 @@ Package: PureCN |
| 2 | 2 |
Type: Package |
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Title: Copy number calling and SNV classification using |
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targeted short read sequencing |
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-Version: 2.13.2 |
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| 6 |
-Date: 2025-03-20 |
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+Version: 2.13.3 |
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+Date: 2025-03-28 |
|
| 7 | 7 |
Authors@R: c(person("Markus", "Riester",
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| 8 | 8 |
role = c("aut", "cre"),
|
| 9 | 9 |
email = "[email protected]", |
| ... | ... |
@@ -1,7 +1,12 @@ |
| 1 | 1 |
Changes in version 2.14.0 |
| 2 | 2 |
------------------------- |
| 3 | 3 |
|
| 4 |
+NEW FEATURES |
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| 5 |
+ |
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+ o Do not filter allosome coverage for male samples. |
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+ |
|
| 4 | 8 |
BUGFIXES |
| 9 |
+ |
|
| 5 | 10 |
o Fixed large runtime of readAllelicCounts. Thanks luyh-xp (#378). |
| 6 | 11 |
o --bai was ignored in Coverage.R except for lists (#272). Thanks |
| 7 | 12 |
@nspies-carisls and @lbeltrame. |
