README

说明

已经不准备在github上继续更新有关文献阅读记录。此间内容会逐步更新到转移到gitbook中。

What is this ?

• 为了让文献阅读更加高效，并且有一项记录，建立了这个项目，会慢慢增加内容。

目录

1. Extrachromosomal oncogene amplification drives tumor evolution and genetic heterogeneity
2. BCFtools/csq: haplotype-aware variant consequences
3. MBV: an efficient sample mislabeling and technical bias detection method for combined genotype and sequencing assay data sets
4. Atherosclerosis Somatic mutations in haematopoietic cells contribute to atherosclerosis
5. Clonal Hematopoiesis and Risk of Atherosclerotic Cardiovascular Disease
6. The genomic landscape of pediatric and young adult T-lineage acute lymphoblastic leukemia
7. Importance of being uncertanin
8. Rare germline variants in ATM are associated with chronic lymphocytic leukemia
9. Error bars
10. Significance, P values and t-tests
11. Points of significance Power and sample size
12. Visualizing samples with box plots
13. Comparing samples—part I
14. Comparing samples—part II
15. Nonparametric tests
16. Designing comparative experiments