Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts

  • GenoMax
    replied
    Originally posted by jevins28 View Post
    My apologies I posted the previous post a bit hastily. I found the common.mk file and altered it as described here http://defsci.blogspot.com/2011/02/c...untu-1004.html

    But when I ran make again I get this error again:

    make[1]: *** [blat] Error 1
    make[1]: Leaving directory `/home/Downloads/blatSrc/blat'
    make: *** [all] Error 2

    However, the make function ran longer than it ever has!

    I'm using ubuntu 64 bit

    any ideas?
    Have you tried "make clean" followed by another try at "make" with the new common.mk file in place?

    Leave a comment:


  • jevins28
    replied
    My apologies I posted the previous post a bit hastily. I found the common.mk file and altered it as described here http://defsci.blogspot.com/2011/02/c...untu-1004.html

    But when I ran make again I get this error again:

    make[1]: *** [blat] Error 1
    make[1]: Leaving directory `/home/Downloads/blatSrc/blat'
    make: *** [all] Error 2

    However, the make function ran longer than it ever has!

    I'm using ubuntu 64 bit

    any ideas?

    Leave a comment:


  • jevins28
    replied
    I'm having the same problem. I can't find the file common.mk on Jim Kent's webpage. Perhaps you could find it again and post the link?

    Thanks

    Leave a comment:


  • ymwur
    replied
    The author of Blat, JIm Knet, just made a updated common.mk file under the inc folder. The new common.mk gets rid of the ependency on libpng. So, now I can install Blat without install libpng. I believe Jim will put the update version in his website soon.
    Thank you for all your help.

    Leave a comment:


  • sklages
    replied
    Be sure to install the corresponding header files, e.g. for libpng12 -> libpng12-dev

    Leave a comment:


  • ymwur
    replied
    I downloaded the libpng and installed it under /usr/local.
    But when I install the BlatSrc and the same error message showed up.
    I think the error occured wheh it try to run the makefile in the blat folder.
    But when I looked this makefile, I could not fine any text spefiying -lpng.

    What can be the problem?
    Thanks,

    Leave a comment:


  • GenoMax
    replied
    For ubuntu you can install the "libpng" package. https://launchpad.net/ubuntu/precise/+source/libpng

    You should be able to use the package manager or do the apt-get install.

    Leave a comment:


  • ymwur
    replied
    Hi

    Thank you for information.
    I am installing BLAT in 64-bit linux system with Ubuntu 12.
    Does lpng also work in linux or is there a similar library for linux?

    Leave a comment:


  • GenoMax
    replied
    You have not said what operating system you are installing blat on (is this cygwin on windows) but I am going to guess that the "-lpng" is referring to this library http://swapped.cc/#!/lpng. You can find the download link at the bottom of the page.

    Leave a comment:


  • ymwur
    started a topic BLAT installtation problem

    BLAT installtation problem

    Hi,

    I am trying to install BLAT. But I encounter a probelm I cannot find solution online.
    I got a error message like below:
    make[1]: Entering directory `/home/joinet/software/blatSrc/blat'
    gcc -O -g -Wall -Wformat -Wimplicit -Wreturn-type -Wuninitialized -o /home/joinet/bin/x86_64/blat blat.o ../lib/x86_64/jkOwnLib.a ../lib/x86_64/jkweb.a -pthread -lpng -lm
    /usr/bin/ld: cannot find -lpng
    collect2: ld 回傳 1
    make[1]: *** [blat] Error 1
    make[1]: Leaving directory `/home/joinet/software/blatSrc/blat'
    make: *** [all] Error 2

    Do anyone tell me how can I fix this probelm?
    Thanks.

    Chih-Ming

Latest Articles

Collapse

  • SEQadmin2
    Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
    by SEQadmin2



    CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

    Despite this, “CRISPR helped turn genome editing from a specialized technique into
    ...
    Yesterday, 11:01 AM
  • SEQadmin2
    Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
    by SEQadmin2


    Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

    The systematic characterization of the human proteome has
    ...
    07-20-2026, 11:48 AM
  • SEQadmin2
    Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
    by SEQadmin2



    Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
    ...
    07-09-2026, 11:10 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, Yesterday, 02:55 AM
0 responses
9 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-24-2026, 12:17 PM
0 responses
12 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-23-2026, 11:41 AM
0 responses
13 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-20-2026, 11:10 AM
0 responses
24 views
0 reactions
Last Post SEQadmin2  
Working...