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Biology版 - 大家都是用什么软件来quantifying fluorescent image?
相关主题
如何用imageJ来quantify fluorescence intensity?大家如何看模式动物的high-throuput phenotyping
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关于imageJ里的min, max and mean。。。谢谢offer求建议
相关话题的讨论汇总
话题: image话题: 软件话题: plot
进入Biology版参与讨论
1 (共1页)
l******g
发帖数: 1145
1
某些原因需要quantify同一张图片上,两个部分的intensity,然后计算ratio(A/B)的
数值。
用什么软件比较方便?最好是免费的软件~
v***a
发帖数: 1242
2
ImageJ~

【在 l******g 的大作中提到】
: 某些原因需要quantify同一张图片上,两个部分的intensity,然后计算ratio(A/B)的
: 数值。
: 用什么软件比较方便?最好是免费的软件~

l******g
发帖数: 1145
3
呃?ImageJ如此万能?我再去钻研钻研,谢~~

【在 v***a 的大作中提到】
: ImageJ~
l******g
发帖数: 1145
4
再问一下,需要装哪个plug-in?
找到一个colour deconvolution plugin,但貌似比较适合HE和DAB staining.

【在 v***a 的大作中提到】
: ImageJ~
r**t
发帖数: 64
5
I also would like ask a question. After having all the bands selected, I
went to “gels ->Plot lanes”, but the pop-up window is vertical instead of
horizontal, making measurement of the peak areas impossible as I can’t see
where to draw the base line of a peak. What do I need to do so that the plot
will be horizontal showing each peak from left to right on the screen (
instead of from top to bottom). What plug-in do I need? Thanks.
s*****j
发帖数: 6435
6
seems you can turn your image 90 degree.

of
see
plot

【在 r**t 的大作中提到】
: I also would like ask a question. After having all the bands selected, I
: went to “gels ->Plot lanes”, but the pop-up window is vertical instead of
: horizontal, making measurement of the peak areas impossible as I can’t see
: where to draw the base line of a peak. What do I need to do so that the plot
: will be horizontal showing each peak from left to right on the screen (
: instead of from top to bottom). What plug-in do I need? Thanks.

1 (共1页)
进入Biology版参与讨论
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如何用imageJ来quantify fluorescence intensity?大家如何看模式动物的high-throuput phenotyping
请教用什么软件可以计算 IHC staining的面积啊?FYI:quantify individual's scientific contribution
如何用ImageJ quantify fluorescence intensities at plasma membrane vs. cytosol?any experience?
Re: How to quantify DNA bands?请问2倍的差异可以用western监测么?
相关话题的讨论汇总
话题: image话题: 软件话题: plot