A Detailed Introduction to the Basic Operation of SerialEM.ppt
《A Detailed Introduction to the Basic Operation of SerialEM.ppt》由会员分享,可在线阅读,更多相关《A Detailed Introduction to the Basic Operation of SerialEM.ppt(28页珍藏版)》请在麦多课文档分享上搜索。
1、A Detailed Introduction to the Basic Operation of SerialEM,Image Buffers in SerialEM,Images are saved in buffers, referred to as A NCamera acquisitions and processed images go into buffer A, and the top few images are rolled into higher buffersTypical situations (enforced during tilt series) are:,A
2、B C D E G H ,New image -,Align reference,Read-in image -,(Home)(Insert) (Delete)(End),Normal operation,New image -,Record reference,Read-in image -,(Home)(Insert) (Delete)(End),Low dose mode,A B C D E F G H ,Trial reference,Image Display Panel,The available data range in the displayed image is contr
3、olled by the Black and White levels: everything outside this range is truncated To determine Black and White, it analyzes pixels in a central area and truncates a certain fraction Contrast and brightness are of limited usefulness because of this truncation Most useful option is to set “Area Fraction
4、” to smaller value, like spot metering on smaller central area To see contrast at extreme end of range, enter image minimum as Black value or image maximum as White value Zoom pretty much takes care of itself with default settings,Microscope Status Panel,Screen current is more useful than exposure t
5、ime; “Float” button floats a screen meter, good when tuning scope “Dose” button floats a cumulative dose meter The Defocus is based on a microscope readout, not the actual focus on the specimen On Tecnai, it matches TUI defocus reading, can be reset in TUI or SerialEM On JEOL, it is arbitrary and se
6、t to zero on program startup, can be reset IS is image shift in microns, important to know on 300KV Tecnai and JEOL 2100 without high power image shift,Tilt Control Panel,The delay time is the delay after tilting by basic increment delay will be longer or shorter for bigger or smaller tilts,Camera a
7、nd Macro Tools,Buttons for camera parameter setup and 5 camera acquisition modes (good for low dose) STOP is the one general stop button for all kinds of operations “Preview” morphs into “Montage” when montaging, unless low dose is on Macro buttons also morph into useful buttons during tilt series,C
8、amera Parameter Setup,Continuous acquisition is only mildly useful (no access to fast camera modes) Processing options useful for testing and troubleshooting; otherwise always use gain normalization Binning is used for speed. Tracking correlations are always binned down to 512 so there is no point t
9、aking Trials bigger than 512. A full-width image gives fastest readout per pixel; hence the wide options for fast subarea pictures A separate dark reference is kept for every binning and exposure time. “Force new dark reference next time” is the way to remove a dark reference Averaging dark referenc
10、es is helpful for a high-noise camera (not typical),Pre-exposure,Pre-exposure (drift settling) requires two shutters The Gatan shuttering mode that allows pre-exposure is inflexible and exposes specimen during readout so SerialEM uses beam blanking to provide selected pre-exposure while blanking dur
11、ing readout “Dual shuttering minimum exposure” mode provides for this and just does beam blanking when drift settling is 0 so it can always be used But the camera timing must be calibrated so the beam blanking does not occur during exposure time Tietz cameras require Shutterbox II for pre-exposure t
12、o work,Image Alignment & Focus,Autoalign always changes microscope image shift “Clear alignment” undoes that “Reset Image Shift” moves the stage to keep the same specimen point centered Moving stage for mouse shifts avoids having to reset image shift Happens automatically if option selected and move
13、ment is above either absolute (micron) or relative (fraction of field) threshold You can do it intentionally with Shift key Trimming dark borders keeps autoalign from being thrown off by beam edge or grid bar Used automatically in low dose and during “tasks” done at lower than working mag Will not d
14、etect less extreme contrast differences that can throw off autoalign alternative is to use smaller area (higher trim fraction) “Center image shift on tilt axis” will give fewer movements during tilt series but requires an offset calibration,Autofocusing with Beam Tilt,Autofocus is done by taking two
15、 images with the beam tilted in opposite directions and measuring the shift between imagesIt relies on the microscope being aligned such that the image of a specimen in the focal plane of the objective lens does not move when the beam is tilted.,A,Specimen in focal plane,Image plane,A appears here w
16、ith both directions of tilt,B,Specimen out of focus,Image plane,B or C appears here depending on direction of tilt,C,Focus Parameters and Operations,The target is the defocus it sets to after measuring The beam tilt needs to be big enough to get good image displacements, but is limited by objective
17、aperture Autofocus Offset lets you measure defocus at focus different from target Can protect against correlation failures by focusing at zero Can be used to focus at a defocus with more contrast Taking three pictures lets it subtract off drift “Drift protection” “Report shift and drift” takes the t
18、hree pictures and just tells you the beam-induced shift and the drift “Report on existing” reports the shift and drift from pictures just acquired “Autofocus” measures and changes to target; “Measure defocus” just measures without changing Autofocus sometimes works poorly at high tilt - “Check autof
19、ocus” assesses what fraction of a known focus change can be detected “Move Focus Center” lets you click on spot at desired focus and change focus so center of field is at that focus,File Operations,You can open new image files or existing files (up to 8 now) Opening a new file brings up File Propert
20、ies dialog, where you set the data type and items to save in header Anything selected for saving can be extracted with extracttilts (options -st, -ma, or -in for stage position, mag, or intensity) After opening an old file, the “Set” options can be used to change the properties that would be set in
21、the File Properties dialog “Save to Other” and “Read from Other” can be used to save one image or read from a file without leaving it open You can save an image to a specific Z value with “Overwrite” Saving a log is useful. “Read & Append” lets you accumulate a log across several runs of the program
22、,Camera Commands,The most commonly used item in the camera menu is “Prepare Gain Reference” Gain reference can be done at typical exposure for non-low dose work Having lots of counts averaged (e.g., 10 x 1/3 of dynamic range) is more important than matching the counts for actual images Binned gain r
23、eference works for normalizing images with even binning useful for slow 4K camera that is being used as 2K camera If camera counts per electron is calibrated, this can do automatic dose calibration It can be useful for troubleshooting to view gain reference or dark reference of image just taken “Pos
24、t-actions” controls whether image shift, mag change, or stage move are taken during camera readout Requires correct camera timing parameters and with that, it is surprisingly robust But it can be turned off to troubleshoot problems,Montaging The Camera Is No Limit,To start montaging, define the numb
- 1.请仔细阅读文档,确保文档完整性,对于不预览、不比对内容而直接下载带来的问题本站不予受理。
- 2.下载的文档,不会出现我们的网址水印。
- 3、该文档所得收入(下载+内容+预览)归上传者、原创作者;如果您是本文档原作者,请点此认领!既往收益都归您。
下载文档到电脑,查找使用更方便
2000 积分 0人已下载
下载 | 加入VIP,交流精品资源 |
- 配套讲稿:
如PPT文件的首页显示word图标,表示该PPT已包含配套word讲稿。双击word图标可打开word文档。
- 特殊限制:
部分文档作品中含有的国旗、国徽等图片,仅作为作品整体效果示例展示,禁止商用。设计者仅对作品中独创性部分享有著作权。
- 关 键 词:
- ADETAILEDINTRODUCTIONTOTHEBASICOPERATIONOFSERIALEMPPT

链接地址:http://www.mydoc123.com/p-373145.html