transPlotR

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关于trackVis的问题

6

我在使用trackVis遇到了一定的问题，我的代码如下： > file data save(data,file = 'Data.rda') > load('Data.rda') > mybw trackVis(bWData = mybw,chr = "Wnk4",region.min = 101167654,region.max = 101168235) 错误信息如下所示： Error in `combine_vars()`: ! Faceting variables must have at...

Zh-MicroSat

error in scan.

3

I use bedVis function to visualize one bed file, then get the error information: > Error in scan(file = file, what = what, sep = sep, quote = quote, dec...

FloodLin

Some problem when using its package

4

1. when I load my bigwig file, it only works on my current work directory， such as : `loadBigWig('../bigwig/my.bigwig')` and get: `Error in $

yuanlizhanshi

any way to show transcript fusion in a large scale

1

Hi Junjun, I am wondering is there any way to show transcript fusion in a large scale. Thanks

Shicheng-Guo

图片文字调整

1

想问一下，如何调节图片基因名字的位置呀，太靠上面了，想往下面移

shaoxiong2588

不能指定范围作图

4

# coding gene trancriptVis(gtfFile = gtf1, Chr = 17, posStart = 36783355, posEnd = 36783400) Error in `map()`: ℹ In index: 1. Caused by error in `dplyr::filter()`: ℹ In argument:...

shaoxiong2588

can this reading vcf file and plot SNV?

2

apxmfrstmc

我使用以下代码：指定线粒体中基因位置 trackVis(bWData = mybw, chr = "chrMT", region.min = 1000, region.max = 2000) 出图如下所示，并没有按照我给定的范围出图：  不知道是什么原因呢

Magetutor