Mercurial > repos > davidvanzessen > shm_csr
annotate shm_selection.htm @ 91:f387cc1580c6 draft
"planemo upload commit 6f5bdb4189fcc9028c90365d8edf8d1d7c1cf690"
author | rhpvorderman |
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date | Wed, 02 Feb 2022 10:57:36 +0000 |
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50 <p class=MsoNormalCxSpFirst style='text-align:justify'><b><span lang=EN-GB | |
51 style='font-size:12.0pt;line-height:115%;font-family:"Times New Roman","serif"'>References</span></b></p> | |
52 | |
53 <p class=MsoNormalCxSpMiddle style='text-align:justify'><span lang=EN-GB | |
54 style='font-size:12.0pt;line-height:115%;font-family:"Times New Roman","serif"; | |
55 color:black'>Yaari, G. and Uduman, M. and Kleinstein, S. H. (2012). Quantifying | |
56 selection in high-throughput Immunoglobulin sequencing data sets. In<span | |
57 class=apple-converted-space> </span><em>Nucleic Acids Research, 40 (17), | |
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58 pp. e134–e134.</em><span class=apple-converted-space><i> </i></span>[</span><span |
67 | 59 lang=EN-GB><a href="http://dx.doi.org/10.1093/nar/gks457" target="_blank"><span |
60 style='font-size:12.0pt;line-height:115%;font-family:"Times New Roman","serif"; | |
61 color:#303030'>doi:10.1093/nar/gks457</span></a></span><span lang=EN-GB | |
62 style='font-size:12.0pt;line-height:115%;font-family:"Times New Roman","serif"; | |
63 color:black'>][</span><span lang=EN-GB><a | |
64 href="http://dx.doi.org/10.1093/nar/gks457" target="_blank"><span | |
65 style='font-size:12.0pt;line-height:115%;font-family:"Times New Roman","serif"; | |
66 color:#303030'>Link</span></a></span><span lang=EN-GB style='font-size:12.0pt; | |
67 line-height:115%;font-family:"Times New Roman","serif";color:black'>]</span></p> | |
68 | |
69 <p class=MsoNormalCxSpMiddle style='text-align:justify'><b><span lang=EN-GB | |
70 style='font-size:12.0pt;line-height:115%;font-family:"Times New Roman","serif"'>Graphs</span></b></p> | |
71 | |
72 <p class=MsoNormalCxSpMiddle style='text-align:justify'><u><span lang=EN-GB | |
73 style='font-size:12.0pt;line-height:115%;font-family:"Times New Roman","serif"'>AA | |
74 mutation frequency</span></u></p> | |
75 | |
76 <p class=MsoNormalCxSpMiddle style='text-align:justify'><span lang=EN-GB | |
77 style='font-size:12.0pt;line-height:115%;font-family:"Times New Roman","serif"'>For | |
78 each class, the frequency of replacement mutations at each amino acid position | |
79 is shown, which is calculated by dividing the number of replacement mutations | |
80 at a particular amino acid position/the number sequences that have an amino | |
81 acid at that particular position. Since the length of the CDR1 and CDR2 region | |
82 is not the same for every VH gene, some amino acids positions are absent. | |
83 Therefore we calculate the frequency using the number of amino acids present at | |
84 that that particular location. </span></p> | |
85 | |
86 <p class=MsoNormalCxSpMiddle style='text-align:justify'><u><span lang=EN-GB | |
87 style='font-size:12.0pt;line-height:115%;font-family:"Times New Roman","serif"'>Antigen | |
88 selection (BASELINe)</span></u></p> | |
89 | |
90 <p class=MsoNormalCxSpMiddle style='text-align:justify'><span lang=EN-GB | |
91 style='font-size:12.0pt;line-height:115%;font-family:"Times New Roman","serif"'>Shows | |
92 the results of the analysis of antigen selection as performed using BASELINe. | |
93 Details on the analysis performed by BASELINe can be found in Yaari et al, | |
94 PMID: 22641856. The settings used for the analysis are</span><span lang=EN-GB | |
95 style='font-size:12.0pt;line-height:115%;font-family:"Times New Roman","serif"'>: | |
96 focused, SHM targeting model: human Tri-nucleotide, custom bounderies. The | |
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"planemo upload commit fd64827ff6e63df008f6f50ddb8576ad2b1dbb26"
rhpvorderman
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97 custom boundries are dependent on the ‘sequence starts at filter’. </span></p> |
67 | 98 |
99 <p class=MsoNormalCxSpMiddle style='line-height:normal'><span lang=NL | |
100 style='font-family:UICTFontTextStyleBody;color:black'>Leader: | |
101 1:26:38:55:65:104:-</span></p> | |
102 | |
103 <p class=MsoNormalCxSpMiddle style='line-height:normal'><span lang=NL | |
104 style='font-family:UICTFontTextStyleBody;color:black'>FR1: 27:27:38:55:65:104:-</span></p> | |
105 | |
106 <p class=MsoNormalCxSpMiddle style='line-height:normal'><span lang=NL | |
107 style='font-family:UICTFontTextStyleBody;color:black'>CDR1: 27:27:38:55:65:104:-</span></p> | |
108 | |
109 <p class=MsoNormalCxSpLast style='line-height:normal'><span lang=NL | |
110 style='font-family:UICTFontTextStyleBody;color:black'>FR2: 27:27:38:55:65:104:-</span></p> | |
111 | |
112 <p class=MsoNormal><span lang=NL style='font-size:12.0pt;line-height:115%; | |
113 font-family:"Times New Roman","serif"'>Hanna IJspeert, Pauline A. van | |
114 Schouwenburg, David van Zessen, Ingrid Pico-Knijnenburg, Gertjan J. Driessen, | |
115 Andrew P. Stubbs, and Mirjam van der Burg (2016). </span><span | |
116 style='font-size:12.0pt;line-height:115%;font-family:"Times New Roman","serif"'>Evaluation | |
117 of the Antigen-Experienced B-Cell Receptor Repertoire in Healthy Children and | |
118 Adults. In <i>Frontiers in Immunolog, 7, pp. e410-410. </i>[<a | |
119 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066086/"><span | |
120 style='color:windowtext'>doi:10.3389/fimmu.2016.00410</span></a>][<a | |
121 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066086/"><span | |
122 style='color:windowtext'>Link</span></a>]</span></p> | |
123 | |
124 </div> | |
125 | |
126 </body> | |
127 | |
128 </html> |